Clinical Trial for the Application of Tirobot System
NCT02890043 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 88
Last updated 2016-09-12
Summary
The object of this study was to evaluate the accuracy and safety of the Tirobot system.
Conditions
- Fusion of Spine (Disease)
- Robotic Surgical Procedures
Interventions
- PROCEDURE
-
robot-assisted spine surgery
robot-assisted spine surgery using Tirobot system
- PROCEDURE
-
free-hand surgery
traditional free-hand surgery
- DEVICE
-
TiRobot system
a robot-assisted spine surgery system
Sponsors & Collaborators
-
Beijing Tinavi Medical Technology Co Ltd
collaborator UNKNOWN -
Chinese PLA General Hospital
collaborator OTHER -
Tianjin Hospital
collaborator OTHER -
Beijing Jishuitan Hospital
lead OTHER
Principal Investigators
-
Wei Tian, MD · Beijing Jishuitan Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-01-31
- Primary Completion
- 2016-06-30
- Completion
- 2016-07-31
Countries
- China
Study Locations
More Related Trials
-
New Robotic Assistance System for Spinal Fusion Surgery
NCT02558621 ·Status: COMPLETED ·Phase: NA
-
Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System
NCT05884593 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Safety and Effectiveness Evaluation of Spinal Laminectomy Robot
NCT06593574 ·Status: RECRUITING ·Phase: NA
-
Clinical Trial of Minimally Invasive Robotic Spine Surgery
NCT02121249 ·Status: COMPLETED ·Phase: NA
-
Prospective Robotic-Guided Registry of Spine Surgery
NCT05181098 ·Status: UNKNOWN
-
Cost-effectiveness Analysis of Robot-assisted Spinal Surgery
NCT05388383 ·Status: UNKNOWN
-
Evaluation on Efficacy of Total Artificial Disc Replacement (TDR) of Cervical Spondylosis
NCT03364816 ·Status: UNKNOWN
-
Study of Individualized, Precise and Standardized Cervical Open-door Surgery for Cervical Spinal Stenosis
NCT05786313 ·Status: RECRUITING ·Phase: NA
-
RPE-P/TLIF for Lumbar Spinal Stenosis With Instability
NCT06290908 ·Status: COMPLETED
-
Safety of MRI Compatible Hardware for MRI-based Image Guidance During Spine Surgery
NCT04563806 ·Status: TERMINATED ·Phase: EARLY_PHASE1
-
Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease
NCT01494441 ·Status: COMPLETED ·Phase: NA
-
Application of 3D Printing Guide Plate in Endoscopic Spinal Surgery
NCT05632835 ·Status: UNKNOWN ·Phase: NA
-
Clinical Study With a Robotic Assistant in Patients Requiring a Spinal Transpedicular Fixation
NCT06153511 ·Status: COMPLETED ·Phase: NA
-
Effectiveness and Safety of Mobile Artificial Cervical Vertebrae Replacement for Patients With Cervical Spondylosis
NCT04813211 ·Status: UNKNOWN ·Phase: NA
-
Advanced SPinal Innovations With Robotics and Enabling Technology Registry
NCT05071144 ·Status: RECRUITING
-
A Clinical Study of a Spine Fusion System in Vertebral Body Fusion Surgery
NCT02252185 ·Status: COMPLETED ·Phase: NA
-
A Muti-Center Study Comparing 3 Procedures for Bi-level Cervical Spondylosis
NCT03358225 ·Status: UNKNOWN
-
A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease
NCT01494428 ·Status: COMPLETED ·Phase: NA
-
Prospective Study of Fusion Rates Using Spira-C Device for Anterior Cervical Discectomy and Fusion Surgery
NCT03786432 ·Status: TERMINATED ·Phase: NA
-
Cortical Bone Trajectory Screws vs. Traditional Pedicle Screws Fixation
NCT03105167 ·Status: UNKNOWN ·Phase: NA
-
Evaluating the Accuracy of Navigation Assisted Pedicle Screw Placement of Spine Surgery
NCT01247948 ·Status: UNKNOWN ·Phase: NA
-
A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc Disease
NCT01491451 ·Status: COMPLETED ·Phase: NA
-
Screening and Prospective Cohort Study of Risk Factors for Enhanced Recovery After Spinal Fusion Surgery in Advanced Age Patient
NCT06591442 ·Status: ENROLLING_BY_INVITATION
-
Comparison of Rigid and Non-Rigid Interbody Fusion Device for Cervical Degenerative Disc Disease in Adults
NCT04550923 ·Status: RECRUITING ·Phase: PHASE4
-
Evaluation of the Fortilink IBF System With TETRAfuse Technology
NCT03699891 ·Status: COMPLETED