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Spinal Stenosis Lumbar clinical trials

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NCT ID: NCT03105167 Recruiting - Clinical trials for Lumbar Disc Herniation

Cortical Bone Trajectory Screws vs. Traditional Pedicle Screws Fixation

Start date: May 7, 2018
Phase: N/A
Study type: Interventional

Transforaminal lumbar interbody fusion (TLIF) had been favorable for effectively decrease pain and disability in specific spinal disorders; however, there has been concern regarding pedicle screw placement during TLIF surgery. Recently, several biomechanical studies had demonstrated that CBT technique achieves screw purchase and strength equivalent to or greater than the traditional method. Furthermore, Only 1 report examined the surgical outcomes of TLIF with CBT screws fixation compared with TLIF using traditional pedicle screws fixation. TLIF with CBT screws fixation may be effective for specific spinal disorders, but the evidence supporting this possibility is still limited.

NCT ID: NCT02982291 Withdrawn - Clinical trials for Spinal Stenosis Lumbar

Focused Spinal Stenosis Rehabilitation Program for Lumbar Spinal Stenosis

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Lumbar spinal stenosis with neurogenic claudication is a common condition in the elderly population and is characterized by bilateral buttock, thigh, or calf discomfort and/or pain, as well as by weakness precipitated by walking and prolonged standing. Self-management options include physical therapy, which includes exercise as a core component for improving the flexibility and mobility of the spine and hips. A Williams flexion protocol has historically been used to treat low-back pain following degenerative changes to the posterior elements of the lumbar spine. However, few studies have been done to validate the efficacy of this protocol. A more focused treatment protocol may be more efficacious. Patients in this study will be randomized to receive either the generic physical therapy protocol (15 sessions) or the focused rehabilitation program (5 sessions). The sessions will take place over the course of 6 months. Outcomes will be assessed using validated questionnaires and physical function tests.

NCT ID: NCT02555280 Recruiting - Clinical trials for Spinal Stenosis Lumbar

Coflex PS3 Actual Conditions for Use Study

PAS003
Start date: September 9, 2019
Phase: N/A
Study type: Interventional

A 2 and 5 year evaluation of clinical outcomes in the treatment of degenerative spinal stenosis with concomitant low back pain by decompression with additional stabilization using the coflex® Interlaminar Technology for FDA Actual Conditions of Use Study.