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Cervical Spine FractureNCT02880839

Digital Navigation Enhances Cervical Pedicle Screw Placement Accuracy and Safety

A study testing Partial cervical lamina excision group, Pipeline-dredge discharge group and Digital navigation group in people with Cervical Spine Fracture, run by Nantong University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

To compare the internal fixation results of three pedicle screw implantation methods and investigated the accuracy and safety of digital navigation-assisted pedicle screw placement. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Cervical Spine Fracture
What is being tested?
Partial cervical lamina excision group, Pipeline-dredge discharge group and Digital navigation group
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
76 participants
Where
No sites listed yet
Study dates
Sep 2013to Dec 2017
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

  • Fracture of the posterior column of the cervical spine or fracture of the anterior-posterior column of the cervical spine without severe vertebral body injury
  • Non-traumatic cervical lamina destabilization, including metastatic tumor and rheumatoid arthritis
  • Kyphotic deformity after cervical lamina resection
  • Segmental destabilization after nerve root or spinal cord decompression
  • Subjected to revision after anterior cervical spine surgery
  • Scheduled to undergo internal fixation by cervical pedicle screw
Show all 9Show fewer
  • Age approximately 62 years
  • Either sex
  • Provision of signed informed consent to participate in the trial

Who cannot join

  • Cervical pedicle injury resulting from trauma or tumor
  • Severe osteoporosis
  • Anatomical variation of the vertebral artery
  • Unable or declined to proceed with internal fixation by pedicle screws

About this study

Official title: Digital Navigation Enhances Cervical Pedicle Screw Placement Accuracy and Safety: A Randomized Controlled Trial

To compare the internal fixation results of three pedicle screw implantation methods and investigated the accuracy and safety of digital navigation-assisted pedicle screw placement.

Read the detailed description

History and current status of related studies

The cervical pedicle is a tiny structure adjacent to important tissues including the spinal cord and vertebral artery. Cervical pedicle screw internal fixation is the conventional treatment for cervical spine fracture, and the technique provides acceptable internal fixation; however, current manipulation methods result in high pedicle screw penetration rates, a high risk of damage to peripheral vessels and nerves, and high rates of postoperative deformity. Improved techniques and minimally invasive methods such as transcutaneous pedicle screw implantation have been designed to effectively reduce surgery-related injury while maintaining the accuracy and safety of pedicle screw implantation. Unfortunately, there is no unified standard regarding implantation of cervical pedicle screws, and many pedicle screw implantation methods are used including partial cervical lamina excision and pipeline-dredge discharge. However, both of these techniques are clinically limited because of poor maneuverability. Digital navigation is an emerging technique based on the discrete-accumulation principle. The technique integrates computer methods, numerical control, laser and new materials, and provides a new digital technique for confirming the location and orientation of cervical pedicle screws, ensuring safe surgical operation.

Features different from other related studies

Previous studies focused primarily on investigating the curative effects of pedicle screw implantation in cervical spine fracture. To the best of the investigators knowledge, there are no studies of cervical spine fracture treatment by digital navigation-assisted cervical pedicle screw placement before June 2006 in Web of Science. The investigators located two similar articles (Cervical Spondylotic Myelopathy Surgical Trial (identifier: NCT02076113) and Slotted Hole Versus Fixed Hole C-Tek (identifier: NCT00585923)) in a search of ClinicalTrials.gov up to June 2006. The outcome measures in these two studies included bony fusion Short Form 36 and the physical component score. In contrast to these two studies regarding inclusion criteria and grouping, the investigators study was designed to investigate the accuracy and safety of digital navigation-assisted cervical pedicle screw placement, hoping to provide valuable quantitative evidence for the clinical application of this technique.

Adverse events

Possible adverse events included any expected or unexpected symptoms. If severe adverse events occurred, their details including the date of occurrence and measures taken to treat the adverse events were reported to the principal investigator and the institutional review board within 24 hours.

Data collection, management, analysis and open access

Data collection: Case report forms with demographic data, disease diagnosis, accompanying diseases, drug allergy history, and adverse events were collected, processed using Epidata software (Epidata Association, Odense, Denmark), collated, and then recorded electronically by data managers using a double-data entry strategy.

Data management: The locked electronic database was accessible and locked only by the project manager, and was not altered. Paper and electronic data regarding screening, informed consent, and clinical outcomes have been preserved at the Affiliated Hospital of Nantong University, China.

Data analysis: The electronic database was statistically analyzed by a professional statistician who created an outcome analysis report that was submitted to the lead researchers. An independent data monitoring committee supervised and managed the trial data, ensuring a scientific and stringent trial to yield accurate and complete data.

Data open access: Anonymized trial data was published at http://www.figshare.com.

Statistical analysis

Statistical analysis was performed by a statistician using SPSS 19.0 software (SPSS Inc.) and followed the intention-to-treat principle. Normally distributed measurement data was expressed as mean, standard deviation, and minimums and maximums. Non-normally distributed measurement data were expressed as lower quartile (q1), and median and upper quartile (q3). The Kruskal-Wallis H-test was used to compare the visual analogue scale spine scores among the three groups, and Fisher's exact test was used to compare the degree of bony fusion of the atlantoaxial joint and the incidence of adverse reactions. P < 0.05 was considered statistically significant.

Being tested
Partial cervical lamina excision group, Pipeline-dredge discharge group, Digital navigation group

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Partial cervical lamina excision groupDevice

    Patients with cervical fracture were assigned to undergo partial cervical lamina excision and cervical pedicle screw internal fixation.

  • Pipeline-dredge discharge groupDevice

    Patients with cervical fracture were assigned to undergo pipeline-dredge discharge and cervical pedicle screw internal fixation.

  • Digital navigation groupDevice

    Also called Digital navigation system

    Patients with cervical fracture were assigned to undergo digital navigation assisted cervical pedicle screw placement.

Study groups in NCT02880839
Study groupRoleWhat they receive
Partial cervical lamina excision groupExperimentalPatients in the cervical lamina partial excision group underwent partial cervical lamina excision and cervical pedicle screw internal fixation.
Receives: Device: Partial cervical lamina excision group
Pipeline-dredge discharge groupExperimentalPatients in the pipeline-dredge discharge group underwent pipeline-dredge discharge and cervical pedicle screw internal fixation.
Receives: Device: Pipeline-dredge discharge group
Digital navigation groupExperimentalPatients in the digital navigation group underwent digital navigation-assisted cervical pedicle placement.
Receives: Device: Digital navigation group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. the penetration degree of the cervical pedicle screws

    According to whether screws penetrated the pedicle and the degree of penetration, screw insertion was graded in three levels: grade I, pedicle screws do not penetrate the pedicular cortex; grade II, screw threads penetrate the cortex at the isthmic portion of the pedicle (no more than 1/4 length of the screw diameter); grade III, screws obviously penetrate the cortex at the isthmic portion of the pedicle (> 1/4 length of the screw diameter) with risk of peripheral nerve and vessel injury, and poor stabilization of the internal fixation.

    Measured: 12 months after internal fixation

Secondary outcomes (4)
  1. bony fusion rate of the atlantoaxial joint

    To evaluate fracture healing. Bone fusion rate in the atlantoaxial joint was calculated as the percentage of patients with bony fusion of the atlantoaxial joint divided by the total patient number in each group.

    Measured: 12 and 36 months after internal fixation

  2. Visual analogue scale spine score

    To evaluate cervical neck pain. The visual analogue scale spine score ranges

    Measured: prior to and 12 and 36 months after internal fixation

  3. American Spinal Injury Association Classification

    To evaluate improvements in neurological function

    Measured: prior to and 12 and 36 months after internal fixation

  4. incidence of adverse events

    To evaluate the safety of each pedicle screw implantation method. The incidence of adverse events was calculated as the percentage of patients developing adverse events divided by the total patient number in each group.

    Measured: 12 and 36 months after internal fixation

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Aug 2016 (estimated)
  2. Study startSep 2013
  3. Primary completionDec 2016 (estimated)
  4. Study completionDec 2017 (estimated)

Resources

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
None (open label)
Enrolment
76 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02880839
Sponsor's protocol ID
NantongU_001
Status last verified
Aug 2016
First submitted
19 Aug 2016
Last updated
26 Aug 2016
Results posted
No
Data monitoring committee
Yes
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Partial cervical lamina excision group, Pipeline-dredge discharge group and Digital navigation group in people with Cervical Spine Fracture, run by Nantong University.

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 9 inclusion and 4 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 26 Aug 2016. Status can change between updates, so confirm with the study contact before making plans.

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?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

the penetration degree of the cervical pedicle screws (time frame: 12 months after internal fixation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 26 Aug 2016.

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