Accuracy Study of Robot-assisted Screw Insertion in Spinal Surgery

Safety and Accuracy of Robot-assisted Versus Fluoroscopy-assisted Screw Insertion in Spinal Surgery: a Prospective Multicenter Randomized Controlled Trial

The investigators present the design of a randomized trial to compare the accuracy and safety of screw insertion using the robot-assisted technique versus the conventional fluoroscopy-assisted technique in spine surgery at multicenter. The accuracy and safety of screw insertion are measured by deviation of guide pin placement position, deviation of screw placement position, and intraoperative or postoperative complications. Secondary outcome parameters such as radiation exposure, postoperative recovery, duration of surgery, length of hospital stay and economic appraisal were also evaluated and compared between treatment groups.

Study Overview

• Status: Unknown
• Conditions: the Robot-assisted Technique
• Intervention / Treatment: Device: the TiRobot system; Device: Freehand

Detailed Description

In spinal surgery, the accurate placement of implants is the key to ensure the success of the surgery, to achieve the safety and clinical requirements of internal fixation. Robot-assisted technology has become an effective means to improve the accuracy of implants with higher accuracy, free from fatigue and equivalent repetitive operation. The investigators present the design of a randomized trial to compare the accuracy and safety of screw insertion using the robot-assisted technique versus the conventional fluoroscopy-assisted technique in spine surgery at multicenter.

500 participants per group (1000 participants in total) are being recruited after diagnosis and before treatment through multi-hospital system and randomised to 1) robot-assisted technique or 2) conventional fluoroscopy-assisted technique in spine surgery. Outcomes are being measured pre-operatively, during- surgery and at 3, 6, 12 months post-surgery. The accuracy and safety of screw insertion are measured by deviation of guide pin placement position, deviation of screw placement position, and intraoperative or postoperative complications. Secondary outcome parameters such as radiation exposure, postoperative recovery, duration of surgery, length of hospital stay and economic appraisal were also evaluated and compared between treatment groups.

The study is addressing key questions of importance by evaluating the TiRobot-assisted technique versus the conventional fluoroscopy-assisted technique in spine surgery at multicenter. Outputs include evidence to facilitate more effective and safe decision making about surgical treatment for spine.

• Study Type: Interventional
• Enrollment (Anticipated): 1000
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Wei Tian, MD. PHD; Phone Number: 86-13901174297; Email: tianwei_victor@163.com
• Study Contact Backup: Name: Mingxing Fan, MD. PHD; Phone Number: 86-13683360600; Email: van0208@163.com

Study Locations

• China
  • Beijing
    • Beijing, Beijing, China, 100035
      • Recruiting
      • Beijing Jishuitan Hospital
      • Contact: Weijun Zhang, MD.; Phone Number: 010-82156660; Email: zhangweijun@tinavi.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years to 78 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• age 18 or above, gender not limited;
• patients eligible for surgery;
• the patient signed the informed consent and agreed to participate in this study.

Exclusion Criteria:

• patients with severe osteoporosis;
• patients with old fractures;
• patients with developmental deformity of the vertebral body with screw placement;
• patients complicated with severe systemic diseases;
• patients with coagulation dysfunction;
• patients deemed unsuitable for the test by the clinical institution.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Other: robot-assisted technique	Device: the TiRobot system; The TiRobot system (TINAVI Medical Technologies Co. Ltd.) is a multi-indication orthopedic surgical robot that can be used in spinal, pelvic, and limb surgeries performed via an open or a minimally invasive approach
Other: conventional fluoroscopy-assisted technique	Device: Freehand; conventional fluoroscopy-assisted

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Deviation of guide pin placement position	After completing guide pin placement preparation, do the C arm scan, obtain 3-D scanning image, plan on the image, position by the robot, finish the needle placement and obtain 3-D scanning image again. Fusion two groups of the image, measure the distance between the entry and exit points of the guide pin and the surgical planning, calculate the insertion deviation, and evaluate the insertion accuracy of the guide pin. Insertion deviation = (Input offset distance + Output offset distance) / 2, the unit is mm. If more than one guide pin is needed for the operation, the deviation of the insertion shall be calculated separately and the average shall be taken.	during operation
Time of guide pin adjustion	After the guide pin is placed, when the position deviation needs to be adjusted, the time consumed by adjusting the guide pin.	during operation
Deviation of screw placement position	Postoperative screw placement position deviation was measured. The position of spinal screws was evaluated by postoperative imaging. Standard for classification of spinal screw placement : Excellent：The screw was completely in the pedicle and did not penetrate the cortex. Good: The screw cortical perforation < 2mm, or less than 50% of the screw diameter. Bad： The screw cortical perforation > 2mm, or more than 50% of the screw diameter.	during operation
Time of screw adjustion	After the screw is placed, when the position deviation needs to be adjusted, the time consumed by adjusting the screw.	during operation
Intraoperative Complications	Intraoperative complications, including but not limited to: positioning complications (blindness, nerve injury, skin breakdown), acute spinal cord injury, vascular Injury(vertebral injury, aorto-iliac injury), cardiovascular events, pulmonary complications, acute kidney injury.	After operation up to 4 weeks
Postoperative Complications	Postoperative complications，including but not limited to: cardiovascular events, pulmonary complications, acute kidney injury, ileus, coagulopathy and wound infection. The time was within 1 year after the operation.	The time was within 1 year after the operation.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Duration of surgery	Duration of surgery refers to the time from the end of anesthesia to the end of the operation. In addition to the total operation time, the time before the screw placement, the time used for the screw placement, the time used for intraoperative decompression or reduction (if any) and the time used for install connecting rod were separately counted.	during operation
Radiation exposure	Measure and calculate the radiation exposure to the patients and clinicians.	during operation
Visual analogue scale (VAS) score 24 hours before surgery	Patients' pain information was evaluated by VAS score. The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.	24 hours before surgery
Visual analogue scale (VAS) score 24 hours after surgery	Patients' pain information was evaluated by VAS score. The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.	24 hours after surgery
Visual analogue scale (VAS) score 3 months after surgery	Patients' pain information was evaluated by VAS score. The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.	3 months after surgery
Visual analogue scale (VAS) score 6 months after surgery	Patients' pain information was evaluated by VAS score. The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.	6 months after surgery
Visual analogue scale (VAS) score 1 year after surgery	Patients' pain information was evaluated by VAS score. The visual analogue scale or visual analog scale (VAS) is a psychometric response scale which can be used in questionnaires. It is a measurement instrument for subjective characteristics or attitudes that cannot be directly measured. When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.	1 year after surgery
JOA score 24 hours before surgery	For patients with cervical vertebra diseases, a 17-point cervical JOA score was used to evaluate the spinal cord function. For patients with lumbar vertebral disease, a 29-point lumbar JOA score was used to evaluate spinal cord function. JOA scores of the patients were collected before surgery, after surgery, and 3 months, 6 months and 1 year postoperatively.	24 hours before surgery
JOA score 24 hours after surgery	For patients with cervical vertebra diseases, a 17-point cervical JOA score was used to evaluate the spinal cord function. For patients with lumbar vertebral disease, a 29-point lumbar JOA score was used to evaluate spinal cord function. JOA scores of the patients were collected before surgery, after surgery, and 3 months, 6 months and 1 year postoperatively.	24 hours after surgery
JOA score 3 months after surgery	For patients with cervical vertebra diseases, a 17-point cervical JOA score was used to evaluate the spinal cord function. For patients with lumbar vertebral disease, a 29-point lumbar JOA score was used to evaluate spinal cord function. JOA scores of the patients were collected before surgery, after surgery, and 3 months, 6 months and 1 year postoperatively.	3 months after surgery
JOA score 6 months after surgery	For patients with cervical vertebra diseases, a 17-point cervical JOA score was used to evaluate the spinal cord function. For patients with lumbar vertebral disease, a 29-point lumbar JOA score was used to evaluate spinal cord function. JOA scores of the patients were collected before surgery, after surgery, and 3 months, 6 months and 1 year postoperatively.	6 months after surgery
JOA score 1 year after surgery	For patients with cervical vertebra diseases, a 17-point cervical JOA score was used to evaluate the spinal cord function. For patients with lumbar vertebral disease, a 29-point lumbar JOA score was used to evaluate spinal cord function. JOA scores of the patients were collected before surgery, after surgery, and 3 months, 6 months and 1 year postoperatively.	1 year after surgery
NDI score 24 hours before surgery	For patients with cervical vertebra diseases, NDI score was used to evaluate cervical spine dysfunction index. Total score from 0 (no disability) to 50 (complete disability).	24 hours before surgery
NDI score 24 hours after surgery	For patients with cervical vertebra diseases, NDI score was used to evaluate cervical spine dysfunction index. Total score from 0 (no disability) to 50 (complete disability).	24 hours after surgery
NDI score 3 months after surgery	For patients with cervical vertebra diseases, NDI score was used to evaluate cervical spine dysfunction index. Total score from 0 (no disability) to 50 (complete disability).	3 months after surgery
NDI score 6 months after surgery	For patients with cervical vertebra diseases, NDI score was used to evaluate cervical spine dysfunction index. Total score from 0 (no disability) to 50 (complete disability).	6 months after surgery
NDI score 1 year after surgery	For patients with cervical vertebra diseases, NDI score was used to evaluate cervical spine dysfunction index. Total score from 0 (no disability) to 50 (complete disability).	1 year after surgery
ODI score 24 hours before surgery	For patients with lumbar vertebra diseases, ODI score was used to evaluate the lumbago related score. The Oswestry Disability Index (ODI) is an index derived from the Oswestry Low Back Pain Questionnaire used by clinicians and researchers to quantify disability for low back pain. 0% -20%: Minimal disability 21%-40%: Moderate Disability 41%-60%: Severe Disability 61%-80%: Crippling back pain 81%-100%: These patients are either bed-bound or have an exaggeration of their symptoms.	24 hours before surgery
ODI score 24 hours after surgery	For patients with lumbar vertebra diseases, ODI score was used to evaluate the lumbago related score. The Oswestry Disability Index (ODI) is an index derived from the Oswestry Low Back Pain Questionnaire used by clinicians and researchers to quantify disability for low back pain. 0% -20%: Minimal disability 21%-40%: Moderate Disability 41%-60%: Severe Disability 61%-80%: Crippling back pain 81%-100%: These patients are either bed-bound or have an exaggeration of their symptoms.	24 hours after surgery
Health related quality of life 3 months after surgery	Health related quality of life is being assessed with the SF-36 that is the most widely used QOL measure in the world with norms for the Australian general population available. The SF-36 contains a mental health and physical health summary scale suitable to measure the impact of the intervention on patients' wellbeing.	3 months after surgery
Health related quality of life 6 months after surgery	Health related quality of life is being assessed with the SF-36 that is the most widely used QOL measure in the world with norms for the Australian general population available. The SF-36 contains a mental health and physical health summary scale suitable to measure the impact of the intervention on patients' wellbeing.	6 months after surgery
Health related quality of life 1 year after surgery	Health related quality of life is being assessed with the SF-36 that is the most widely used QOL measure in the world with norms for the Australian general population available. The SF-36 contains a mental health and physical health summary scale suitable to measure the impact of the intervention on patients' wellbeing.	1 year after surgery
Economic appraisal	Costs for each arm of the trial will be analysed by components of the intervention pathway (e.g. pre-consultation, work-up, theatre, post-treatment, follow-up, management/coordination, side-effects, etc.); by expenditure category (e.g. capital, staff, consumables, overheads, other); and by incidence (i.e. who bears the costs). The cost component of the economic appraisal will thus assess the cost drivers from a range of perspectives for both intervention approaches. Downstream costs and potential cost offsets incurred beyond the randomized trial data collection period will be modelled from the literature and expert opinion, with sources clearly documented.	The time was within 1 year after the operation.
length of hospital stay	Length of hospital stay refers to the time from the first day of hospitalization to the discharge after surgery.	Up to the 4 weeks

Collaborators and Investigators

• Sponsor: Beijing Jishuitan Hospital

Publications and helpful links

General Publications

• Fan M, Fang Y, Zhang Q, Zhao J, Liu B, Tian W. A prospective cohort study of the accuracy and safety of robot-assisted minimally invasive spinal surgery. BMC Surg. 2022 Feb 11;22(1):47. doi: 10.1186/s12893-022-01503-4.

Study record dates

Study Major Dates

• Study Start (Actual): March 1, 2019
• Primary Completion (Anticipated): March 1, 2020
• Study Completion (Anticipated): June 1, 2020

Study Registration Dates

• First Submitted: April 10, 2019
• First Submitted That Met QC Criteria: July 31, 2019
• First Posted (Actual): August 1, 2019

Study Record Updates

• Last Update Posted (Actual): August 1, 2019
• Last Update Submitted That Met QC Criteria: July 31, 2019
• Last Verified: July 1, 2019

More Information

Terms related to this study

• Other Study ID Numbers: JST-201903

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No