SpondylolisthesisNCT02998060
Clinical Evidence of Robot Guided vs. Navigated vs. Free Hand Lumbar Spinal Fusion
A study testing Pedicle Screw Placement, SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) and 3D C-Arm (Ziehm Imaging, Nuremberg, Germany) in people with Spondylolisthesis and Intervertebral Disc Degeneration, run by Marc Schröder at 2 sites in 2 countries.
Trial summary
Computer-based navigation systems were first introduced to spine surgery in 1995 and while they have been long established as standards in certain cranial procedures, they have not been similarly adopted in spine surgery. Read more about this study
- Who is it for?
- Ages 17 to 79 years
- Conditions the study is for
- Spondylolisthesis, Intervertebral Disc Degeneration
- What is being tested?
- Pedicle Screw Placement, SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) and 3D C-Arm (Ziehm Imaging, Nuremberg, Germany)
- Type of treatment
- Medical device, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 0 participants
- Where
- 2 sitesin 2 countries
- Study dates
- 1 Jan 2019to May 2019
- 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 17 to 79 years
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Informed Consent
- Lumbar single level discopathy or Spondylolisthesis of Meyerding Grade 1 or 2
- Body Mass Index >19 and <33
- American Society of Anesthesiologists Scale 1 or 2
Who cannot join
- Severe Scoliosis (Coronal Cobb's >30 degrees / Schwab classification sagittal modifier + or ++)
Trial locations and contacts
2 sites in 2 countries.
2 sites in 2 countries
Germany1 site
Universitätsmedizin Göttingen Georg-August
Göttingen, Lower Saxony, 37075
About this study
Computer-based navigation systems were first introduced to spine surgery in 1995 and while they have been long established as standards in certain cranial procedures, they have not been similarly adopted in spine surgery. Designed to overcome some of the limitations of navigation-based technologies, robot-guided surgical systems have become commercially available to surgeons worldwide.These systems are rapidly challenging the gold standards.
The aim is to conduct a prospective randomized controlled trial. The randomized variable will be the screw placement technique used. One arm will be treated with lumbar fusion using robotic guidance (RG), one arm will receive the same procedure but with a free hand technique (FH) and the third arm will use navigation (NV) (CT or Fluoroscopy-assisted). Intraoperative screw revisions and revision surgery for screw malposition as well as clinical patient-reported outcomes to identify any such differences between these methods of screw insertion will be assessed.
Read the detailed description
A decade ago, minimally invasive surgery (MIS) was considered a promising development in spine surgery, yet the value of the pioneering technologies was questionable. With the growing number of experienced MIS surgeons, the influx of evidence in favour of MIS is rapidly increasing. This makes a compelling argument towards MIS offering distinct clinical benefits over open approaches in terms of blood loss, length of stay, rehabilitation, cost-effectiveness and perioperative patient comfort. Due to the limited or inexistent line-of-sight in MIS procedures, surgeons need to rely on imaging, navigation, and guidance technologies to operate in a safe and efficient manner. Therefore, a plethora of new and ever improving navigational systems have been developed. These systems allow a consistent level of safety and accuracy, on par with results achieved by very experienced free hand surgeons, with a reasonably short learning curve.
Computer-based navigation systems were first introduced to spine surgery in 1995 and while they have been long established as standards in certain cranial procedures, they have not been similarly adopted in spine surgery. Designed to overcome some of the limitations of navigation-based technologies, robot-guided surgery has become commercially available to surgeons worldwide, like SpineAssist® (Mazor Robotics Ltd. Caesarea, Israel) and the recently launched ROSA™ Spine (Zimmer-Biomet, Warsaw, Indiana, USA). These systems are rapidly challenging the gold standards.
SpineAssist®, and its upgraded version, the Renaissance®, provides a stable drilling platform and restricts the surgeon's natural full range of motion to 2 degrees of freedom (up/down motion and yaw in the cannula). The system's guidance unit moves into the trajectory based on exact preoperative planning of pedicle screws, while accounting for changes in intervertebral relationships such as due to distraction, cage insertion or changes between the supine patient position in the preoperative CT and the prone patient on the operating table. Published evidence on robot-guided screw placement has demonstrated high levels of accuracy with most reports ranging around 98% of screws placed within the pedicle or with a cortical encroachment of less than 2 mm.
Although the reliability and accuracy of robot-guided spine surgery have been established, the actual benefits for the patient in terms of clinical outcomes and revision surgeries remain unknown.
The investigators recently conducted a cohort study that showed some evidence that robotic guidance lowers the rate of intraoperative screw revisions and implant related reoperations compared to free hand procedures, while achieving comparable clinical outcomes. Now, these factors, among others, have to be assessed on a higher level of evidence. This would be, to date, the first randomized controlled trial comparing clinical patient reported outcomes of robotic guided (RG) pedicle screw placement vs. navigated (NV) vs. free hand (FH) pedicle screw placement.
The investigator's aim is to conduct a prospective randomized controlled trial. The randomized variable will be the screw placement technique used. One arm will be treated with lumbar fusion using robotic guidance (RG), one arm will receive the same procedure but with a free hand technique (FH) and the third arm will use navigation (NV) (CT or Fluoroscopy-assisted).
- Being tested
- Pedicle Screw Placement, SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel), 3D C-Arm (Ziehm Imaging, Nuremberg, Germany)
- Keywords
- Robot, Spinal Fusion, Spine, Navigation, Freehand
- Medical subject headings
- Spondylolisthesis, Intervertebral Disc Degeneration
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Pedicle Screw PlacementProcedure or surgery
As a part of the lumbar spinal fusion procedure, posterior pedicle screws will be placed.
SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel)Device
This robot will be used to guide pedicle screws into their trajectories.
3D C-Arm (Ziehm Imaging, Nuremberg, Germany)Device
This 3D Fluoroscope will be used to navigate pedicle screws into their trajectories.
| Study group | Role | What they receive |
|---|---|---|
| Robot-guided | Active comparator | Robotic guidance (SpineAssist®or Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) will be used for navigation and insertion of pedicle screws. Receives: Procedure: Pedicle Screw Placement; Device: SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) |
| Navigated | Active comparator | A computer-assisted method of navigation (CT- or 3D-Fluoroscopy-based) will be used for navigation and insertion of pedicle screws. Receives: Procedure: Pedicle Screw Placement; Device: 3D C-Arm (Ziehm Imaging, Nuremberg, Germany) |
| Freehand | Active comparator | Pedicle screws will be inserted using the freehand technique under fluoroscopic control. Receives: Procedure: Pedicle Screw Placement |
What is being measured
The primary outcome is the main question the study is designed to answer.
Quality of Life after Spinal Fusion as assessed using the Euroqol EQ-5D questionnaire
Measured: 12 months after surgery
Back Pain after Spinal Fusion as assessed using the Oswestry Disability Index (ODI)
Measured: 12 months after surgery
Back and Leg pain after Spinal Fusion as assessed using a Virtual Analogue Scale (VAS)
Measured: 12 months after surgery
Secondary outcomes (2)
Number of Pedicle Screws that needed intraoperative Revision
If a pedicle screw is malpositioned and this is noticed intraoperatively, the screw can be removed and revised.
Measured: Intraoperatively (From induction until end of anesthesia)
Number of Revision Surgeries for malpositioned Screws
If a screw malposition is not detected intraoperatively and neurological deficits or other complaints secondary to the malpositioned screw arise, the screw needs to be surgically revised.
Measured: Through study completion, an average of 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Dec 2016 (estimated)
- Study start1 Jan 2019 (estimated)
- Primary completionMar 2019 (estimated)
- Study completionMay 2019 (estimated)
Why it stopped: Change in study design \[Randomization not feasible\]
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SpondylolisthesisStudies of the same condition, open and under way.
- 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
- None (open label)
- Enrolment
- 0 participants (actual)
Sponsor and investigators
- Lead sponsor
- Marc Schröder
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Marc Schröder, Bergman Clinics
- Investigators
- Victor E Staartjes, Stud. Med., Principal investigator, University of Zurich
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02998060
- Sponsor's protocol ID
- ABR-59636
- Status last verified
- Oct 2018
- First submitted
- 11 Dec 2016
- Last updated
- 22 Oct 2018
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Oct 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Evidence of Robot Guided vs. Navigated vs. Free Hand Lumbar Spinal Fusion
- ClinicalTrials.gov ID
- NCT02998060
- Acronym / sponsor ID
- ABR-59636
- Keywords
- Robot, Spinal Fusion, Spine, Navigation, Freehand
- Study type
- Interventional
- Recruitment status
- WithdrawnReason stopped: Change in study design \[Randomization not feasible\]
- Enrolment
- 0 participants (actual)
- Lead sponsor
- Marc SchröderUniversity, hospital or other
- Study start
- 1 Jan 2019 (estimated)
- Primary completion
- Mar 2019 (estimated)
- Study completion
- May 2019 (estimated)
- First posted
- 20 Dec 2016 (estimated)
- 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.
Computer-based navigation systems were first introduced to spine surgery in 1995 and while they have been long established as standards in certain cranial procedures, they have not been similarly adopted in spine surgery. Designed to overcome some of the limitations of navigation-based technologies, robot-guided surgical systems have become commercially available to surgeons worldwide.These systems are rapidly challenging the gold standards.
The aim is to conduct a prospective randomized controlled trial. The randomized variable will be the screw placement technique used. One arm will be treated with lumbar fusion using robotic guidance (RG), one arm will receive the same procedure but with a free hand technique (FH) and the third arm will use navigation (NV) (CT or Fluoroscopy-assisted). Intraoperative screw revisions and revision surgery for screw malposition as well as clinical patient-reported outcomes to identify any such differences between these methods of screw insertion will be assessed.
Detailed description
A decade ago, minimally invasive surgery (MIS) was considered a promising development in spine surgery, yet the value of the pioneering technologies was questionable. With the growing number of experienced MIS surgeons, the influx of evidence in favour of MIS is rapidly increasing. This makes a compelling argument towards MIS offering distinct clinical benefits over open approaches in terms of blood loss, length of stay, rehabilitation, cost-effectiveness and perioperative patient comfort. Due to the limited or inexistent line-of-sight in MIS procedures, surgeons need to rely on imaging, navigation, and guidance technologies to operate in a safe and efficient manner. Therefore, a plethora of new and ever improving navigational systems have been developed. These systems allow a consistent level of safety and accuracy, on par with results achieved by very experienced free hand surgeons, with a reasonably short learning curve.
Computer-based navigation systems were first introduced to spine surgery in 1995 and while they have been long established as standards in certain cranial procedures, they have not been similarly adopted in spine surgery. Designed to overcome some of the limitations of navigation-based technologies, robot-guided surgery has become commercially available to surgeons worldwide, like SpineAssist® (Mazor Robotics Ltd. Caesarea, Israel) and the recently launched ROSA™ Spine (Zimmer-Biomet, Warsaw, Indiana, USA). These systems are rapidly challenging the gold standards.
SpineAssist®, and its upgraded version, the Renaissance®, provides a stable drilling platform and restricts the surgeon's natural full range of motion to 2 degrees of freedom (up/down motion and yaw in the cannula). The system's guidance unit moves into the trajectory based on exact preoperative planning of pedicle screws, while accounting for changes in intervertebral relationships such as due to distraction, cage insertion or changes between the supine patient position in the preoperative CT and the prone patient on the operating table. Published evidence on robot-guided screw placement has demonstrated high levels of accuracy with most reports ranging around 98% of screws placed within the pedicle or with a cortical encroachment of less than 2 mm.
Although the reliability and accuracy of robot-guided spine surgery have been established, the actual benefits for the patient in terms of clinical outcomes and revision surgeries remain unknown.
The investigators recently conducted a cohort study that showed some evidence that robotic guidance lowers the rate of intraoperative screw revisions and implant related reoperations compared to free hand procedures, while achieving comparable clinical outcomes. Now, these factors, among others, have to be assessed on a higher level of evidence. This would be, to date, the first randomized controlled trial comparing clinical patient reported outcomes of robotic guided (RG) pedicle screw placement vs. navigated (NV) vs. free hand (FH) pedicle screw placement.
The investigator's aim is to conduct a prospective randomized controlled trial. The randomized variable will be the screw placement technique used. One arm will be treated with lumbar fusion using robotic guidance (RG), one arm will receive the same procedure but with a free hand technique (FH) and the third arm will use navigation (NV) (CT or Fluoroscopy-assisted).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Robot-guided | Active comparator | Procedure: Pedicle Screw Placement, Device: SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel)Robotic guidance (SpineAssist®or Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) will be used for navigation and insertion of pedicle screws. |
| Navigated | Active comparator | Procedure: Pedicle Screw Placement, Device: 3D C-Arm (Ziehm Imaging, Nuremberg, Germany)A computer-assisted method of navigation (CT- or 3D-Fluoroscopy-based) will be used for navigation and insertion of pedicle screws. |
| Freehand | Active comparator | Procedure: Pedicle Screw PlacementPedicle screws will be inserted using the freehand technique under fluoroscopic control. |
Who may qualify
- Ages
- 17 to 79 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (4 listed)
- Informed Consent
- Lumbar single level discopathy or Spondylolisthesis of Meyerding Grade 1 or 2
- Body Mass Index >19 and <33
- American Society of Anesthesiologists Scale 1 or 2
Key exclusion criteria (1 listed)
- Severe Scoliosis (Coronal Cobb's >30 degrees / Schwab classification sagittal modifier + or ++)
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 |
|---|---|---|
| Pedicle Screw PlacementAs a part of the lumbar spinal fusion procedure, posterior pedicle screws will be placed. | Procedure or surgery | Freehand, Navigated, Robot-guided |
| SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel)This robot will be used to guide pedicle screws into their trajectories. | Device | Robot-guided |
| 3D C-Arm (Ziehm Imaging, Nuremberg, Germany)This 3D Fluoroscope will be used to navigate pedicle screws into their trajectories. | Device | Navigated |
Primary outcome
Quality of Life after Spinal Fusion as assessed using the Euroqol EQ-5D questionnaire
Time frame: 12 months after surgery
Back Pain after Spinal Fusion as assessed using the Oswestry Disability Index (ODI)
Time frame: 12 months after surgery
Back and Leg pain after Spinal Fusion as assessed using a Virtual Analogue Scale (VAS)
Time frame: 12 months after surgery
2 secondary outcomes
Number of Pedicle Screws that needed intraoperative Revision
Time frame: Intraoperatively (From induction until end of anesthesia)
Number of Revision Surgeries for malpositioned Screws
Time frame: Through study completion, an average of 12 months
Results and safety
The study was withdrawn before enrolling participants, so there are no results.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Oct 2018.
- Individual participant dataSharing planned: No
Related trials for Spondylolisthesis
Recruiting
Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device
Degenerative Conditions of the Lumbar Spine, Lumbar Spinal Stenosis
RecruitingObservational study
Thoracic-Lumbar Arthrodesis- Implanet Jazz
Spondylolisthesis, Spinal Stenosis
Recruiting
Studying Melatonin and Recovery in Teens
Juvenile; Scoliosis, Scoliosis Idiopathic
Not yet recruiting
Kore Fiber PLF Study
Degenerative Lumbar Spine Diseases, Lumbar Degenerative Disc Disease
Active, not recruiting
SLIP II Registry: Spinal Laminectomy Versus Instrumented Pedicle Screw Fusion
Lumbar Spondylolisthesis, Grade 1 Spondylolisthesis
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.
Victor E Staartjes, Stud. Med. principal investigator
University of Zurich
2 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Pedicle Screw Placement, SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) and 3D C-Arm (Ziehm Imaging, Nuremberg, Germany) in people with Spondylolisthesis and Intervertebral Disc Degeneration, run by Marc Schröder at 2 sites in 2 countries.
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 4 inclusion and 1 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: withdrawn, as of the sponsor's last update on 22 Oct 2018. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Germany, Switzerland. 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?
The study was withdrawn before enrolling participants, so there are no results.
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?
Quality of Life after Spinal Fusion as assessed using the Euroqol EQ-5D questionnaire (time frame: 12 months after surgery). The study lists 3 primary outcomes in all. 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 22 Oct 2018.