Spinal FractureNCT03316703
Surgical Treatment of the Thoracolumbar Spine Fractures.
A study testing Conventional open surgery and Minimally invasive percutaneous surgery in people with Spinal Fracture and Traumatic Fracture, run by University of Sao Paulo at 1 site in Brazil.
Trial summary
The thoracolumbar segment fractures are the most frequent along the spine, and surgical treatment is indicated in unstable fractures. Surgical treatment has been performed through the posterior fixation pedicle fixation systems, and where necessary complemented by decompression of the spinal arthrodesis and previous… Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Spinal Fracture, Traumatic Fracture
- What is being tested?
- Conventional open surgery and Minimally invasive percutaneous surgery
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteBrazil
- Study dates
- 9 May 2018to 1 Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Single level fracture
- Fracture T11-L5
- Posterior Stabilization Indication
Who cannot join
- Fracture in more than 1 level
- Osteoporotic fracture
- Pathological fracture
- Previous history of surgery
- Deformity
- Mental disease
- TCE
- Posterior vertebral canal open decompression
Trial locations and contacts
1 site in 1 country.
Brazil1 site, 1 recruiting
- Recruiting
Hospital das Clinicas.University of Sao Paulo
Ribeirão Preto, São Paulo, 14.048-900
Helton LA Defino, MD, PhD., +55 16 3315-4593, hladefin@fmrp.usp.br
About this study
Official title: Surgical Treatment of the Thoracolumbar Spine Fractures - Conventional Open Surgery Versus Minimally Invasive Percutaneous Surgery: A Randomized Trial.
The thoracolumbar segment fractures are the most frequent along the spine, and surgical treatment is indicated in unstable fractures. Surgical treatment has been performed through the posterior fixation pedicle fixation systems, and where necessary complemented by decompression of the spinal arthrodesis and previous channel. Surgical treatment has been performed by conventional open approach through the posterior incision on the midline, and detachment and removal of paraspinal muscles to access the posterior vertebral elements. The percutaneous minimally invasive surgery was introduced in the context of spinal surgery to reduce the morbidity associated with conventional open approach. It has been reported the lowest bleeding intra- and postoperative period, less pain, shorter hospital stay, rehabilitation and return to work faster with less use of minimally invasive percutaneous approach of the spine. However, predominates in the literature of clinical case reports and few prospective and randomized clinical trials. The performance of prospective randomized clinical trials have been required for the evaluation of the benefits of minimally invasive surgery in the treatment of the thoracolumbar spine fractures. The objective of the study is to compare the surgical treatment of fractures of the thoracolumbar spine using the conventional open approach or minimally invasive percutaneous approach to the stabilization of the vertebral segment affected, and using similar type of pedicle spinal fixation system. Patients will be evaluated in the preoperative, postoperative, 1,2,3,6,12 and 24 months by parameters related to the perioperative (intraoperative bleeding, surgery time), clinical (VAS, SF-36, HADS, EQ-5D-5L), images (radiographs and computed tomography). The study results will impact the guidelines of the surgical treatment of thoracolumbar spine fractures and may indicate the advantages or disadvantages of using surgery through conventional open approach to minimally invasive percutaneous surgery.
Read the detailed description
Introduction: Fractures of the thoracic and lumbar spine are the most frequent fractures of the axial skeleton, and correspond to about 89% of vertebral fractures. Two-thirds of these fractures occur in the thoracolumbar transition between T11 and L2 (50% of thoracic spine fractures at T12 level and 60% of lumbar spine fractures at L1 level). Surgical treatment of thoracolumbar spine fractures has been indicated in unstable fractures with the aim of stabilizing the fractured vertebral segment and allowing early rehabilitation without the use of external immobilization and rest in the bed. Conventional surgical treatment has been performed by means of fixation and posterior arthrodesis of the vertebral segment using pedicle fixation systems with or without arthrodesis The scientific challenge of the project is to carry out this method of pioneering study in our country, as no prospective randomized clinical trial has been performed in our country to compare the outcome of surgical treatment of thoracolumbar spine fractures through conventional open surgery or surgery Minimally invasive percutaneous. There are few reports of prospective and randomized trials on this subject and its implementation has been stimulated to increase the level of evidence related to the surgical treatment of thoracolumbar spine fractures.
The objective of the study will be to compare the results of treatment of thoracolumbar spine fractures through the open approach (conventional surgery) or percutaneous (minimally invasive) approach with a pedicle fixation system without vertebral arthrodesis.
The hypothesis of the study is that minimally invasive percutaneous surgery has the advantage of producing less surgical trauma with less intra- and postoperative bleeding, lower pain intensity, shorter hospitalization time and lower rate of complications, and postero-lateral arthrodesis Is not required in the treatment of thoracolumbar spine fractures.
Material and methods
After the clinical and radiographic evaluation (simple radiographs, CT and MRI if necessary) of the patients the fracture will be classified according to the classification Magerl et al., and the therapeutic planning defined. Fractures with surgical indication by means of the posterior approach will be selected for the study and the randomization process performed individually for each type of fracture (A, B and C) according to the Magerl classification. Patients will be randomized and assigned to two groups: A - conventional open surgery and B - minimally invasive percutaneous surgery.
Surgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae, screws will be used up to the vertebral body and in fractured vertebra shorter screws that do not penetrate the vertebral body will be used. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra.
The vertebral fixation system will be applied through the conventional open approach (group A) or minimally invasive percutaneous approach (group B) according to allocation after randomization.
Patients will be evaluated through perioperative, clinical, and radiographic parameters.
Perioperative parameters:
Time of surgery - time elapsed between incision and closure of the skin. Intraoperative bleeding - a measure of the amount of blood evaluated by the amount of blood drawn and blood from the compresses and gauzes used.
Postoperative bleeding - a measure of the amount of blood aspirated through the drain and measured in the postoperative gauze pads and dressings.
Time of use of fluoroscopy. Postoperative walking time Length of hospital stay Drugs used in the postoperative period
Clinical parameters:
Visual pain scale (VAS) - evaluated in the preoperative period, 1,2,3,4,5,6,7 postoperative days, 1,2,3,6,12 and 24 months.
Medical Outcomes Study 36 - Item Short - Form Health Survey (SF-36) HADS - Hospital Anxiety Depression Scale EQ-5D-5L Dennis Pain and Work Scale Pain Assessment Scale (Dennis) P1: absence of pain P2: minimal occasional pain; No need for medication. P3: Moderate pain, occasional medication and no interruption of professional or daily activities.
P4: moderate or severe pain, occasional absence of work, significant change in daily activities.
P5: constant, severe pain, use of chronic analgesic medication
Work ability assessment scale (Dennis) W1: return to previous work (heavy arm activity) or heavy physical activities W2: return to previous work (sedentary) or heavy physical labor with restrictions W3: unable to return previous plus works full time in another activity W4: unable to return full time to work W5: does not work, totally disabled They were evaluated in the immediate postoperative period, 1,2,3,6,12 and 24 months.
Radiographic Parameters Simple radiographs in AP and profile - location, fracture classification, assessment of vertebral body height, evaluation of Farcy's sagittal index, fractured kyphosis, fractured vertebral kyphosis, intervertebral disc height above and below fractured vertebra, alignment in AP, (preoperative, immediate postoperative, 1,2,3,6,12 and 24 months).
Alignment in the coronal plane will be performed by measuring the angle of Cobb between the line parallel to the proximal vertebral plaque of the vertebra above the fractured vertebra and distal vertebral plate below the fractured vertebra.
The height of the vertebral body will be evaluated by means of the percentage of compression of the vertebral body in relation to the adjacent segments. The height of the vertebral body above (V1) and below (V2) of the fractured vertebra (V3) is considered using the following formula:% compression = [(A1 + A3) / 2-A2] / (A1 + A3) / 2
The kyphosis of the fractured segment will be assessed by the angle formed by the line parallel to the superior vertebral plate of the vertebra proximal to the fractured vertebra and by the line of the inferior vertebral plate of the vertebra distal to the fractured vertebra The sagittal index of the fractured segment (Farcy Index) will be calculated using the height of the proximal vertebra (A1), height of the fractured vertebra (A2) and height of the distal vertebra. Sagittal index of the fractured segment = (A3): 100- (2xA2 / A1 + A3) x100.
Computed tomography - morphology and type of fracture, percentage of compression of the vertebral canal, positioning of the screws (preoperative and immediate postoperative).
Compression of the vertebral canal will be evaluated by measuring the sagittal diameter of the vertebral canal (Fig. 8) and the direct measurement of the cross-sectional area of the vertebral canal using scanning to delimit its perimeter.
The positioning of the screws inside the pedicles will be evaluated by means of tomographic cuts of 2mm. Correct positioning will be considered when the pedicle screw is fully encircled by the vertebral pedicle and the cortical vertebra is not perforated. The perforation will be classified as small (≤2mm), medium (2.1-4mm) and severe (> 4mm), and the perforation site: medial, lateral, superior, posterior will also be evaluated.
Evaluation of implant release, implant breakage and fracture consolidation, loss of reduction.
Computed tomography - evaluation of the paravertebral musculature - Evaluation of the transverse sectional area and fat infiltration in the paravertebral musculature by computed tomography (CT).
The CT examinations performed to evaluate the position of the metallic implants, fracture type and the evolution of the morphology of the vertebral body will also be used to evaluate the paravertebral musculature. In this way it will be possible to compare the effect of each of the fixation techniques on the musculature trophism.
The evaluation will be performed by a senior radiologist with more than fifteen years of experience in musculoskeletal radiology and with experience in evaluation using quantitative techniques.
Patient images will be anonymized and presented to the radiologist through the Osirix imaging software at random. The observer will not be aware of the clinical and surgical information at the time of the measurements to be performed.
Two other researchers, a radiologist and a spine surgeon will perform this classification independently, so as to enable the analysis of Interobserver reproducibility of the classification.
General risks, local and adverse effects - risks will be defined as any incident, change in treatment or normal progress regardless of whether or not it is associated with the treatment being evaluated. The predicted risks related to thoracolumbar spine fractures and their surgical treatment are superficial infection, deep infection, epidural hematoma, duramater injury, inadequate position of pedicle screws, radiculopathy, fractured vertebral segment kyphosis, instability, pain uncontrollable to treatment , Failure of implants, degeneration of adjacent segments, pressure ulcers and reoperation.
The adverse effects will be considered as any undesirable medical event that the study participant presents (death, deep venous thrombosis, septicemia, pulmonary embolism, pneumonia, urinary tract infection, acute respiratory failure, multiple organ failures, hospitalization, prolonged failure of the implants Or intraoperative adverse effects).
- Conditions
- Spinal Fracture, Traumatic Fracture
- Being tested
- Conventional open surgery, Minimally invasive percutaneous surgery
- Keywords
- Spine, Spinal injuries, Fractures, Bone
- Medical subject headings
- Spinal Fractures, Spinal Injuries, Fractures, Bone
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Conventional open surgeryProcedure or surgery
Surgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae to the vertebrae, screws will be used up to the vertebral body and fractured vertebra will use shorter screws that do not penetrate the vertebral body. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra.
The vertebral fixation system will be applied through the conventional open approach (group A).
Minimally invasive percutaneous surgeryProcedure or surgery
Surgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae to the vertebrae, screws will be used up to the vertebral body and fractured vertebra will use shorter screws that do not penetrate the vertebral body. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra.
The vertebral fixation system will be applied through the minimally invasive percutaneous approach (group B) according to allocation after randomization.
| Study group | Role | What they receive |
|---|---|---|
| Conventional open surgery | Active comparator | Fixation of a proximal vertebra, a vertebra distal to the fractured vertebra, and also of the fractured vertebra with a pedicle fixation system using the conventional open to implant placement without subsequent arthrodesis. Receives: Procedure: Conventional open surgery |
| Minimally invasive percutaneous surgery | Experimental | Fixation of a proximal vertebra, a vertebra distal to the fractured vertebra, and also of the fractured vertebra with a pedicle fixation system using the percutaneous minimally invasive approach to implant placement without subsequent arthrodesis. Receives: Procedure: Minimally invasive percutaneous surgery |
What is being measured
The primary outcome is the main question the study is designed to answer.
Postoperative pain
The intensity of pain will be measured by Visual Analogue Scale (VAS).
Measured: up to 24 months
Secondary outcomes (17)
Postoperative complications
To evaluate the rate of postoperative complications such as superficial infection, deep infection, nerve injury, vascular injury, hematoma
Measured: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Postoperative adverse events
The adverse effects will be considered as any undesirable medical event that the study participant presents (death, deep venous thrombosis, septicemia, pulmonary embolism, pneumonia, urinary tract infection, acute respiratory failure, multiple organ failure, hospitalization, prolonged failure of the implants or intraoperative adverse effects).
Measured: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Breakage or release of implants through radiographs
Evaluation of implant release
Measured: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Breakage or release of implants through CT scan
Evaluation of implant release
Measured: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Total costs
The incremental budgetary impact (IO inc) [(NiND x CtND) - (NiDA x CtDA), where NIND = number of patients under percutaneous approach; CtND = total cost of percutaneous approach; NiDA = number of patients in conventional surgery; CtDA =. Total cost of conventional approach.
Measured: 24 months
Intraoperative bleeding (ml)
Intraoperative bleeding - a measure of the amount of blood evaluated by the amount of blood drawn and blood from the compresses and gauzes used.
Measured: 48 hours postoperative
Postoperative bleeding (ml)
Postoperative bleeding - a measure of the amount of blood aspirated through the drain and measured in the postoperative gauze pads and dressings.
Measured: 48 hours postoperative
Surgery time (in minutes)
Time of surgery - time elapsed between incision and closure of the skin.
Measured: Intraoperative
Length of hospital stay (in days)
Number of days stayed in hospital
Measured: At discharge (up to two week post-surgery)
Short Form Health Survey (SF-36)
Patient-reported survey of patient health. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Scores range from 0 - 100. The lower the score the more disability, while the higher the score the less disability.
Measured: 1,2,3,6,12 and 24 months.
Hospital Anxiety Depression Scale (HADS)
Self-rating scale that measures anxiety and depression. The HADS aims to measure symptoms of anxiety and depression and consists of 14 items, seven items for the anxiety subscale (HADS Anxiety) and seven for the depression subscale (HADS Depression). Each item is scored on a response-scale with four alternatives ranging between 0 and 3. All answered are summed to obtain the two subscales. Cut-off scores are 8-10 for doubtful cases and ≥11 for definite cases.
Measured: 1,2,3,6,12 and 24 months.
EuroQol five-dimensional questionnaire (EQ-5D-5L)
Quality of life measure. The EQ-5D-5L has five domain scales (mobility, self-care, usual activities, pain and discomfort, and anxiety and depression) and five levels for each domain. Level 1 response represents "no problems," level 2 "slight problems," level 3 "moderate problems," level 4 "severe problems," and level 5 "extreme problems" or "unable to perform," which is the worst response in the dimension. Also, respondents rate their health on a visual analogue scale ranging from 0 (the worst health imaginable) to 100 (the best health imaginable).
Measured: 1,2,3,6,12 and 24 months.
Vertebral segment kyphosis
The kyphosis of the fractured segment will be assessed by the angle formed by the line parallel to the superior vertebral plate of the vertebra proximal to the fractured vertebra and by the line of the inferior vertebral plate of the vertebra distal to the fractured vertebra. The kyphosis of the fractured vertebra will be assessed by the angle formed by the line parallel to the upper and lower vertebral plate of the fractured vertebra using radiographs and computed tomography.
Measured: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Fractured vertebral body height
The height of the vertebral body will be evaluated by means of the percentage of compression of the vertebral body in relation to the adjacent segments using radiographs and computed tomography. The height of the vertebral body above (V1) and below (V2) of the fractured vertebra (V3) is considered using the following formula:% compression = [(A1 + A3) / 2-A2] / (A1 + A3) / 2
Measured: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Compression of the vertebral canal
Compression of the vertebral canal will be evaluated by measuring the sagittal diameter of the vertebral canal and the direct measurement of the cross-sectional area of the vertebral canal using scanning to delimit its perimeter. The sagittal diameter of the vertebral canal was defined as the distance between the posterior and anterior border of the vertebral canal.
Measured: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Accuracy of the pedicle screws
The positioning of the screws inside the pedicles will be evaluated by means of tomographic cuts of 2mm. Correct positioning will be considered when the pedicle screw is fully encircled by the vertebral pedicle and the cortical vertebra is not perforated.
Measured: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Intraoperative fluoroscopy time (in minutes)
Time of use of fluoroscopy
Measured: Intraoperative
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Oct 2017
- Study start9 May 2018
- Primary completion10 Dec 2021 (estimated)
- Study completion1 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Spinal FractureStudies of the same condition, open and under way.
- More trials run by University of Sao PauloThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Sao Paulo
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Helton Defino, University of Sao Paulo
- Investigators
- Helton LA Defino, MD, PhD., Principal investigator, Department of Orthopedics and Traumatology.University of Sao Paulo
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03316703
- Sponsor's protocol ID
- Thoracolumbar Spine Surgery
- Status last verified
- Sep 2021
- First submitted
- 19 May 2017
- Last updated
- 6 Oct 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Defino HLA, Costa HRT, Nunes AA, Nogueira Barbosa M, Romero V. Open versus minimally invasive percutaneous surgery for surgical treatment of thoracolumbar spine fractures- a multicenter randomized controlled trial: study protocol. BMC Musculoskelet Disord. 2019 Aug 31;20(1):397. doi: 10.1186/s12891-019-2763-1.
PubMed 31472691
Study at a glance
From the registry record, last updated by the sponsor on 6 Oct 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Surgical Treatment of the Thoracolumbar Spine Fractures - Conventional Open Surgery Versus Minimally Invasive Percutaneous Surgery: A Randomized Trial.
- ClinicalTrials.gov ID
- NCT03316703
- Acronym / sponsor ID
- Thoracolumbar Spine Surgery
- Conditions
- Spinal Fracture, Traumatic Fracture
- Keywords
- Spine, Spinal injuries, Fractures, Bone
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- University of Sao PauloUniversity, hospital or other
- Study start
- 9 May 2018 (actual)
- Primary completion
- 10 Dec 2021 (estimated)
- Study completion
- 1 Dec 2023 (estimated)
- First posted
- 20 Oct 2017 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The thoracolumbar segment fractures are the most frequent along the spine, and surgical treatment is indicated in unstable fractures. Surgical treatment has been performed through the posterior fixation pedicle fixation systems, and where necessary complemented by decompression of the spinal arthrodesis and previous channel. Surgical treatment has been performed by conventional open approach through the posterior incision on the midline, and detachment and removal of paraspinal muscles to access the posterior vertebral elements. The percutaneous minimally invasive surgery was introduced in the context of spinal surgery to reduce the morbidity associated with conventional open approach. It has been reported the lowest bleeding intra- and postoperative period, less pain, shorter hospital stay, rehabilitation and return to work faster with less use of minimally invasive percutaneous approach of the spine. However, predominates in the literature of clinical case reports and few prospective and randomized clinical trials. The performance of prospective randomized clinical trials have been required for the evaluation of the benefits of minimally invasive surgery in the treatment of the thoracolumbar spine fractures. The objective of the study is to compare the surgical treatment of fractures of the thoracolumbar spine using the conventional open approach or minimally invasive percutaneous approach to the stabilization of the vertebral segment affected, and using similar type of pedicle spinal fixation system. Patients will be evaluated in the preoperative, postoperative, 1,2,3,6,12 and 24 months by parameters related to the perioperative (intraoperative bleeding, surgery time), clinical (VAS, SF-36, HADS, EQ-5D-5L), images (radiographs and computed tomography). The study results will impact the guidelines of the surgical treatment of thoracolumbar spine fractures and may indicate the advantages or disadvantages of using surgery through conventional open approach to minimally invasive percutaneous surgery.
Detailed description
Introduction: Fractures of the thoracic and lumbar spine are the most frequent fractures of the axial skeleton, and correspond to about 89% of vertebral fractures. Two-thirds of these fractures occur in the thoracolumbar transition between T11 and L2 (50% of thoracic spine fractures at T12 level and 60% of lumbar spine fractures at L1 level). Surgical treatment of thoracolumbar spine fractures has been indicated in unstable fractures with the aim of stabilizing the fractured vertebral segment and allowing early rehabilitation without the use of external immobilization and rest in the bed. Conventional surgical treatment has been performed by means of fixation and posterior arthrodesis of the vertebral segment using pedicle fixation systems with or without arthrodesis The scientific challenge of the project is to carry out this method of pioneering study in our country, as no prospective randomized clinical trial has been performed in our country to compare the outcome of surgical treatment of thoracolumbar spine fractures through conventional open surgery or surgery Minimally invasive percutaneous. There are few reports of prospective and randomized trials on this subject and its implementation has been stimulated to increase the level of evidence related to the surgical treatment of thoracolumbar spine fractures.
The objective of the study will be to compare the results of treatment of thoracolumbar spine fractures through the open approach (conventional surgery) or percutaneous (minimally invasive) approach with a pedicle fixation system without vertebral arthrodesis.
The hypothesis of the study is that minimally invasive percutaneous surgery has the advantage of producing less surgical trauma with less intra- and postoperative bleeding, lower pain intensity, shorter hospitalization time and lower rate of complications, and postero-lateral arthrodesis Is not required in the treatment of thoracolumbar spine fractures.
Material and methods
After the clinical and radiographic evaluation (simple radiographs, CT and MRI if necessary) of the patients the fracture will be classified according to the classification Magerl et al., and the therapeutic planning defined. Fractures with surgical indication by means of the posterior approach will be selected for the study and the randomization process performed individually for each type of fracture (A, B and C) according to the Magerl classification. Patients will be randomized and assigned to two groups: A - conventional open surgery and B - minimally invasive percutaneous surgery.
Surgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae, screws will be used up to the vertebral body and in fractured vertebra shorter screws that do not penetrate the vertebral body will be used. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra.
The vertebral fixation system will be applied through the conventional open approach (group A) or minimally invasive percutaneous approach (group B) according to allocation after randomization.
Patients will be evaluated through perioperative, clinical, and radiographic parameters.
Perioperative parameters:
Time of surgery - time elapsed between incision and closure of the skin. Intraoperative bleeding - a measure of the amount of blood evaluated by the amount of blood drawn and blood from the compresses and gauzes used.
Postoperative bleeding - a measure of the amount of blood aspirated through the drain and measured in the postoperative gauze pads and dressings.
Time of use of fluoroscopy. Postoperative walking time Length of hospital stay Drugs used in the postoperative period
Clinical parameters:
Visual pain scale (VAS) - evaluated in the preoperative period, 1,2,3,4,5,6,7 postoperative days, 1,2,3,6,12 and 24 months.
Medical Outcomes Study 36 - Item Short - Form Health Survey (SF-36) HADS - Hospital Anxiety Depression Scale EQ-5D-5L Dennis Pain and Work Scale Pain Assessment Scale (Dennis) P1: absence of pain P2: minimal occasional pain; No need for medication. P3: Moderate pain, occasional medication and no interruption of professional or daily activities.
P4: moderate or severe pain, occasional absence of work, significant change in daily activities.
P5: constant, severe pain, use of chronic analgesic medication
Work ability assessment scale (Dennis) W1: return to previous work (heavy arm activity) or heavy physical activities W2: return to previous work (sedentary) or heavy physical labor with restrictions W3: unable to return previous plus works full time in another activity W4: unable to return full time to work W5: does not work, totally disabled They were evaluated in the immediate postoperative period, 1,2,3,6,12 and 24 months.
Radiographic Parameters Simple radiographs in AP and profile - location, fracture classification, assessment of vertebral body height, evaluation of Farcy's sagittal index, fractured kyphosis, fractured vertebral kyphosis, intervertebral disc height above and below fractured vertebra, alignment in AP, (preoperative, immediate postoperative, 1,2,3,6,12 and 24 months).
Alignment in the coronal plane will be performed by measuring the angle of Cobb between the line parallel to the proximal vertebral plaque of the vertebra above the fractured vertebra and distal vertebral plate below the fractured vertebra.
The height of the vertebral body will be evaluated by means of the percentage of compression of the vertebral body in relation to the adjacent segments. The height of the vertebral body above (V1) and below (V2) of the fractured vertebra (V3) is considered using the following formula:% compression = [(A1 + A3) / 2-A2] / (A1 + A3) / 2
The kyphosis of the fractured segment will be assessed by the angle formed by the line parallel to the superior vertebral plate of the vertebra proximal to the fractured vertebra and by the line of the inferior vertebral plate of the vertebra distal to the fractured vertebra The sagittal index of the fractured segment (Farcy Index) will be calculated using the height of the proximal vertebra (A1), height of the fractured vertebra (A2) and height of the distal vertebra. Sagittal index of the fractured segment = (A3): 100- (2xA2 / A1 + A3) x100.
Computed tomography - morphology and type of fracture, percentage of compression of the vertebral canal, positioning of the screws (preoperative and immediate postoperative).
Compression of the vertebral canal will be evaluated by measuring the sagittal diameter of the vertebral canal (Fig. 8) and the direct measurement of the cross-sectional area of the vertebral canal using scanning to delimit its perimeter.
The positioning of the screws inside the pedicles will be evaluated by means of tomographic cuts of 2mm. Correct positioning will be considered when the pedicle screw is fully encircled by the vertebral pedicle and the cortical vertebra is not perforated. The perforation will be classified as small (≤2mm), medium (2.1-4mm) and severe (> 4mm), and the perforation site: medial, lateral, superior, posterior will also be evaluated.
Evaluation of implant release, implant breakage and fracture consolidation, loss of reduction.
Computed tomography - evaluation of the paravertebral musculature - Evaluation of the transverse sectional area and fat infiltration in the paravertebral musculature by computed tomography (CT).
The CT examinations performed to evaluate the position of the metallic implants, fracture type and the evolution of the morphology of the vertebral body will also be used to evaluate the paravertebral musculature. In this way it will be possible to compare the effect of each of the fixation techniques on the musculature trophism.
The evaluation will be performed by a senior radiologist with more than fifteen years of experience in musculoskeletal radiology and with experience in evaluation using quantitative techniques.
Patient images will be anonymized and presented to the radiologist through the Osirix imaging software at random. The observer will not be aware of the clinical and surgical information at the time of the measurements to be performed.
Two other researchers, a radiologist and a spine surgeon will perform this classification independently, so as to enable the analysis of Interobserver reproducibility of the classification.
General risks, local and adverse effects - risks will be defined as any incident, change in treatment or normal progress regardless of whether or not it is associated with the treatment being evaluated. The predicted risks related to thoracolumbar spine fractures and their surgical treatment are superficial infection, deep infection, epidural hematoma, duramater injury, inadequate position of pedicle screws, radiculopathy, fractured vertebral segment kyphosis, instability, pain uncontrollable to treatment , Failure of implants, degeneration of adjacent segments, pressure ulcers and reoperation.
The adverse effects will be considered as any undesirable medical event that the study participant presents (death, deep venous thrombosis, septicemia, pulmonary embolism, pneumonia, urinary tract infection, acute respiratory failure, multiple organ failures, hospitalization, prolonged failure of the implants Or intraoperative adverse effects).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Conventional open surgery | Active comparator | Procedure: Conventional open surgeryFixation of a proximal vertebra, a vertebra distal to the fractured vertebra, and also of the fractured vertebra with a pedicle fixation system using the conventional open to implant placement without subsequent arthrodesis. |
| Minimally invasive percutaneous surgery | Experimental | Procedure: Minimally invasive percutaneous surgeryFixation of a proximal vertebra, a vertebra distal to the fractured vertebra, and also of the fractured vertebra with a pedicle fixation system using the percutaneous minimally invasive approach to implant placement without subsequent arthrodesis. |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Single level fracture
- Fracture T11-L5
- Posterior Stabilization Indication
Key exclusion criteria (8 listed)
- Fracture in more than 1 level
- Osteoporotic fracture
- Pathological fracture
- Previous history of surgery
- Deformity
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Conventional open surgerySurgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae to the vertebrae, screws will be used up to the vertebral body and fractured vertebra will use shorter screws that do not penetrate the vertebral body. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra. The vertebral fixation system will be applied through the conventional open approach (group A). | Procedure or surgery | Conventional open surgery |
| Minimally invasive percutaneous surgerySurgical treatment will be performed by stabilizing the fractured vertebral segment (proximal vertebra and vertebra distal to fractured vertebra and fractured vertebra) by means of a 6.5 mm or 6.5 mm diameter polyaxial pedicle screw system. In the fractured proximal and distal vertebrae to the vertebrae, screws will be used up to the vertebral body and fractured vertebra will use shorter screws that do not penetrate the vertebral body. In the fractured vertebra, single or bilateral pedicle screw will be used according to the degree of involvement of the pedicle of the fractured vertebra. The vertebral fixation system will be applied through the minimally invasive percutaneous approach (group B) according to allocation after randomization. | Procedure or surgery | Minimally invasive percutaneous surgery |
Primary outcome
Postoperative pain
Time frame: up to 24 months
The intensity of pain will be measured by Visual Analogue Scale (VAS).
17 secondary outcomes
Postoperative complications
Time frame: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Postoperative adverse events
Time frame: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Breakage or release of implants through radiographs
Time frame: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Breakage or release of implants through CT scan
Time frame: immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Total costs
Time frame: 24 months
Intraoperative bleeding (ml)
Time frame: 48 hours postoperative
Postoperative bleeding (ml)
Time frame: 48 hours postoperative
Surgery time (in minutes)
Time frame: Intraoperative
Length of hospital stay (in days)
Time frame: At discharge (up to two week post-surgery)
Short Form Health Survey (SF-36)
Time frame: 1,2,3,6,12 and 24 months.
Hospital Anxiety Depression Scale (HADS)
Time frame: 1,2,3,6,12 and 24 months.
EuroQol five-dimensional questionnaire (EQ-5D-5L)
Time frame: 1,2,3,6,12 and 24 months.
Vertebral segment kyphosis
Time frame: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Fractured vertebral body height
Time frame: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Compression of the vertebral canal
Time frame: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Accuracy of the pedicle screws
Time frame: preoperative, immediate postoperative, and 1,2,3,6,12 and 24 months of followup
Intraoperative fluoroscopy time (in minutes)
Time frame: Intraoperative
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Oct 2021.
- Derived from this study: PubMed 31472691Defino HLA, Costa HRT, Nunes AA, Nogueira Barbosa M, Romero V. Open versus minimally invasive percutaneous surgery for surgical treatment of thoracolumbar spine fractures- a multicenter randomized controlled trial: study protocol. BMC Musculoskelet Disord. 2019 Aug 31;20(1):397. doi: 10.1186/s12891-019-2763-1.
- Open versus minimally invasive percutaneous surgery for surgical treatment of thoracolumbar spine fractures- a multicenter randomized controlled trial: study protocolLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Helton LA Defino, MD, PhD. principal investigator
Department of Orthopedics and Traumatology.University of Sao Paulo
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Conventional open surgery and Minimally invasive percutaneous surgery in people with Spinal Fracture and Traumatic Fracture, run by University of Sao Paulo at 1 site in Brazil.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 6 Oct 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Brazil. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Helton LA Defino, MD,PhD. (+55 16 36022513, hladefin@fmrp.usp.br), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Postoperative pain (time frame: up to 24 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03316703, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2021.