Clinical trials: Spinal Stenosis
Lumbar Spinal Stenosis
Sensory Integration Therapy Training in Patients With Lumbar Spinal Stenosis
Lumbar spinal stenosis is a common degenerative disease in the elderly. Patients are often accompanied by paresthesias and decreased musculoskeletal system functions, resulting in disability and increasing the burden of medical…
- Trial name
- NCT05425667
- Testing
- virtual reality walking training
- Where
- Taiwan
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- National Taiwan University Hospital
Degenerative Disc Disease, Spondylolisthesis
Safety and Efficacy of the CarboFix Pedicle Screw System
The purpose of this study is to evaluate the safety and efficacy of CarboFix' Pedicle Screw System in the lumbar spine.
- Conditions
- Degenerative Disc Disease, Spondylolisthesis, Spinal Stenosis, Spinal Curvatures
- Trial name
- NCT02039232
- Testing
- Pedicle screw system
- Where
- 2 sites in Israel
- Volunteers
- 46 people
- Sponsor
- CarboFix Orthopedics Ltd.
Lumbar Spinal Stenosis
Comparison of the Order of Treatment in Lumbar Spinal Stenosis
Patients with back pain with spinal stenosis of the lower back will be asked to volunteer for this research study. These patients don't need immediate surgery for this problem.
- Trial name
- NCT02103543
- Testing
- physical therapy, lumbar interlaminar epidural steroid injection, epidural steroid injection
- Where
- United States
- Sponsor
- Emory University
Lumbar Spinal Stenosis, Lumbar Disc Herniation
Safety and Effectiveness Evaluation of Spinal Laminectomy Robot
The purpose of this clinical trial is to evaluate the effectiveness and safety of this spinal robot in assisting doctors to perform laminectomy in spinal surgery under the premise of ensuring the safety of the subjects and…
- Trial name
- NCT06593574
- Testing
- Robotic laminectomy, Traditional laminectomy
- Where
- 3 sites in China
- Volunteers
- 70 people
- Sponsor
- Peking University Third Hospital
Spine Fusion, Lumbar Spondylolisthesis
Titanium vs. PEEK Fusion Devices in 1 Level TLIF
The objective of this study is to evaluate and follow the clinical and radiographic outcomes of patients undergoing 1 level TLIF randomized to either a titanium or a PEEK spacer to 24 months after surgery.
- Conditions
- Spine Fusion, Lumbar Spondylolisthesis, Lumbar Stenosis
- Trial name
- TLIF (NCT05691062)
- Testing
- Titanium Fusion Device, PEEK Fusion Device
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- Twin Cities Spine Center