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AzTrials

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.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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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
What is being tested?
Pedicle Screw Placement, SpineAssist®/Renaissance® (Mazor Robotics Ltd. Caesarea, Israel) and 3D C-Arm (Ziehm Imaging, Nuremberg, Germany)
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

Other trials in Germany

Switzerland1 site
  • University Hospital Geneva

    Geneva, 1205

Other trials in Switzerland

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 groups in NCT02998060
Study groupRoleWhat they receive
Robot-guidedActive comparatorRobotic 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)
NavigatedActive comparatorA 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)
FreehandActive comparatorPedicle 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.

  1. Quality of Life after Spinal Fusion as assessed using the Euroqol EQ-5D questionnaire

    Measured: 12 months after surgery

  2. Back Pain after Spinal Fusion as assessed using the Oswestry Disability Index (ODI)

    Measured: 12 months after surgery

  3. Back and Leg pain after Spinal Fusion as assessed using a Virtual Analogue Scale (VAS)

    Measured: 12 months after surgery

Secondary outcomes (2)
  1. 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)

  2. 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.

  1. First posted20 Dec 2016 (estimated)
  2. Study start1 Jan 2019 (estimated)
  3. Primary completionMar 2019 (estimated)
  4. Study completionMay 2019 (estimated)

Why it stopped: Change in study design \[Randomization not feasible\]

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
0 participants (actual)
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

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.

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