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| Name | Class |
|---|---|
| Uppsala University Hospital | OTHER |
| Ôrebro University Hospital | UNKNOWN |
| Umeå University | OTHER |
| University Hospital, Umeå |
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This prospective multicenter observational cohort study evaluates robotic-assisted pedicle screw placement compared with non-robotic-assisted techniques in spinal surgery. Primary objectives include screw placement accuracy, operative learning curve, and reoperation rate within 2 years.
Pedicle screw fixation is widely used in spinal surgery. Screw misplacement may cause complications and reoperations. Robotic-assisted systems aim to improve accuracy and workflow; however, high-quality real-world evidence regarding long-term clinical outcomes and cost-effectiveness remains limited.
This nationwide cohort study includes consecutive patients undergoing spinal surgery with pedicle screws. Exposure is robotic-assisted versus non-robotic-assisted (navigation-assisted or freehand) screw placement. Data capture is made from registries, radiographs and hospital data. Follow-up is up to 2 years for the primary outcomes and up to 5 years for the secondary outcomes.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Robotic-assisted pedicle screw placement | Robotic-assisted pedicle screw placement using commercially available robotic systems |
| |
| Conventional pedicle screw placement | Conventional pedicle screw placement using navigation-assisted or freehand techniques |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Robotic-assisted pedicle screw placement | Device | Robotic-assisted pedicle screw placement using commercially available robotic systems |
|
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients in which at least one pedicle screw is not accurately placed (substudy 1) | Accurate screw placement is defined as a pedicle screw that remains entirely within the cortical boundary of the pedicle, or with up to 2 mm breach of the pedicle wall (corresponds to Gertzbein-Robbins Grade A and B), assessed on a computed tomography. To evaluate screw placement accuracy, we will define a binary per-patient outcome: whether at least one screw is not accurately placed. The planned sample size for this substudy is 75 patients in the robotic-assisted surgery group, and 426 patients in the non-robotic-assisted group, for a total of 501 patients. For this outcome, previously treated cases may be included as specified in the approved protocol. | Periprocedural |
| Learning curve (substudy 2) | To evaluate the learning curve associated with robotic-assisted surgery, we will model operative time as a function of case number. Operative time is expected to decrease with experience, then plateau. We will use mixed-effects piece-wise linear regression with the surgeon as a random effect to estimate the case number at which operative time levels off. The sample size in this substudy is 100 robotic-assisted spine surgeries in each of the 3 centers currently using robotic-assisted spine surgery (Umeå, Örebro, Uppsala), in total 300 surgeries. For this outcome, previously treated cases may be included as specified in the approved protocol. | Periprocedural |
| Reoperation rate at 2 years (substudy 3) | The primary outcome is the occurrence of reoperations of any cause within 2 years from the index surgery. The expected reoperation rate in the non-robotic group is likely to be higher than 3-5% over a 2-year period, and may in the robotic-assisted group be 1% or less. A difference of 2 percentage points or greater is considered clinically meaningful. Power analyses (80% power, alpha 0.05) have been made in two scenarios, with reoperation rates of 3% vs 1%, or 5% vs 3%. We estimate a ratio of 1:6 for robotic-assisted surgery vs navigation-assisted or free hand surgeries. Comparing 3% and 1% reoperation rates, 420 robotic-assisted surgery patients and 2,520 non-robotic surgery patients are needed (yielding a total sample size of 2,940 patients). In case reoperation rates are 5% and 3%, 866 robotic-assisted surgery patients and 5,196 non-robotic surgery patients are needed (yielding a total sample size of 6,062 patients). |
| Measure | Description | Time Frame |
|---|---|---|
| Screw placement precision | We will evaluate screw placement precision as the deviation between preoperative planning and actual placement in robotic-assisted surgery cases. For each screw, linear deviation (at the tip and tail) perpendicular from the planned position, to the actual position, and angular deviation between the planned position and the actual position will be measured. This comparison will be made on an overlay of the preoperative planning made on a preoperative computed tomography, and compared with the computed tomography performed intra- or postoperative for assessment of pedicle screw position |
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Inclusion Criteria:
Exclusion Criteria:
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Swedish residents undergoing spine surgery in Sweden
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Paul Gerdhem, MD, PhD | Contact | +46(0)186110000 | paul.gerdhem@uu.se | |
| Luigi Belcastro, RN | Contact | +46(0)184710000 | luigi.belcastro@uu.se |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Sahlgrenska university hospital | Recruiting | Gothenburg | Sweden |
Individual participant data underlying the results reported in this study will not be publicly shared. Under Swedish law, registry-based health data are protected by the General Data Protection Regulation (GDPR). Sharing of individual-level data requires a valid ethical approval from the Swedish Ethical Review Authority and a formal data-sharing agreement with the data-holding authority.
Researchers who obtain appropriate ethical approval and fulfill Swedish legal requirements may request access to relevant data from the responsible data controller. Such requests will be evaluated in accordance with national legislation and institutional policies.
The study investigators will share aggregated results and statistical code upon reasonable request.
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot | Yes | No | No | Study Protocol | Feb 2, 2026 | Feb 24, 2026 | Prot_000.pdf |
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| ID | Term |
|---|---|
| D013122 | Spinal Diseases |
| ID | Term |
|---|---|
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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| OTHER |
| Karolinska Institutet | OTHER |
| Karolinska University Hospital | OTHER |
| Stockholm South General Hospital | OTHER |
| Sahlgrenska University Hospital | OTHER |
| University of Linköping | UNKNOWN |
| University Hospital, Linkoeping | OTHER |
| Lund University | OTHER |
| Skane University Hospital | OTHER |
| Länssjukhuset Ryhov | UNKNOWN |
| Länssjukhuset Kalmar | UNKNOWN |
| Örebro University, Sweden | OTHER |
| Göteborg University | OTHER |
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| From enrolment up until 2 years after surgery |
| Periprocedural |
| Length of stay | Inhospital stay (days) for the index surgery | Periprocedural |
| Time to return to work | Time to return to work from the enrolment, which is the time for the index surgery | From surgery until 2 years after surgery |
| Health economic analysis | From enrollment until the two-year follow-up |
| EQ-VAS | Health related quality of life measured with EQ-VAS (ranges from 0 (worst) to 100 (best)) | At the one-year follow-up |
| EQ-5D | Quality of life assessed with EQ-5D, converted into an index, ranging from around 0 (worst) to 1 (best) | At the one-year follow-up |
| Proportion of patients achieving the patient acceptable symptom state (PASS) for EQ-VAS | PASS EQ-VAS is for elective patients 75 or more, and for non-elective patients 65 or more. EQ-VAS ranges from 0 (worst) to 100 (best) | At the one-year follow-up |
| Adverse events- thromboembolic and cardiovascular complications | Number (proportion) of thromboembolic events and cardiovascular complications will be assessed as secondary safety outcomes. | From enrolment until the 2 year follow-up |
| Adverse events- mortality | Mortality will be assessed as a secondary safety outcome. | From enrolment until the 2 year follow-up |
| Ryhov hospital | Recruiting | Jönköping | Sweden |
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| Länssjukhuset Kalmar | Recruiting | Kalmar | Sweden |
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| University Hospital Linköping | Recruiting | Linköping | Sweden |
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| Örebro University Hospital | Recruiting | Örebro | Sweden |
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| Karolinska University Hospital | Recruiting | Stockholm | Sweden |
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| South General Hospital (Södersjukhuset) | Recruiting | Stockholm | Sweden |
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| Umeå University Hospital | Recruiting | Umeå | Sweden |
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| Uppsala University Hospital | Recruiting | Uppsala | 75185 | Sweden |
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