Development and application of a robotic system for endoscopic spine surgery
Research on Key Technology Development and Clinical Application of Small Interactive Spinal Endoscopic Surgery Robot
This study is testing a new robotic system for spine surgery to see if it can help patients with back problems feel better after their surgery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years to 85 Years |
| Sex | All |
| Sponsor | Beijing Jishuitan Hospital Academic / other |
| Locations | 1 site (Beijing, Beijing) |
| Trial ID | NCT06480214 on ClinicalTrials.gov |
What this trial studies
This study investigates the relationship between the extent of decompression achieved during endoscopic spine surgery and patient outcomes one year post-surgery. It focuses on developing a robotic platform that enhances the precision and safety of minimally invasive spinal procedures. By analyzing data from a multicenter cohort of patients with lumbar spinal stenosis and disc herniation, the study aims to establish a comprehensive treatment system that improves clinical outcomes. The research addresses the challenges faced by surgeons in navigating the complexities of spinal anatomy during surgery.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 with lumbar spinal stenosis or disc herniation who have not responded to conservative treatment for at least three months.
Not a fit: Patients with a history of lumbar surgery, spinal instability, or those unable to follow up post-surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and recovery for patients undergoing endoscopic spine surgery.
How similar studies have performed: While robotic assistance in spinal surgery is emerging, this specific approach to endoscopic surgery is relatively novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients with lumbar spinal stenosis or lumbar disc herniation with narrow central canal and lateral recess of single lumbar vertebra; 2. formal conservative treatment is ineffective for at least 3 months; 3. Voluntary surgery and follow-up for more than 6 months; 4. Sign informed consent. 5. The patient is \> 18 years old and has the ability to act autonomously. Exclusion Criteria: 1. Previous history of lumbar surgery; 2, combined with lumbar spondylolisthesis, lumbar instability or spinal deformity; 3, there are surgical contraindications, can not perform surgery; 4, can not follow up on time after surgery or lost visitors.
Where this trial is running
Beijing, Beijing
- Beijing Jishuitan Hospital, Capital Medical University — Beijing, Beijing, China (Recruiting)
Study contacts
- Study coordinator: Yajun Liu
- Email: drliuyajun@163.com
- Phone: 139 1187 8647
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.