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Lumbar Disc Herniation clinical trials

View clinical trials related to Lumbar Disc Herniation.

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NCT ID: NCT04017403 Recruiting - Knee Osteoarthritis Clinical Trials

Probiotics Attenuate Postoperative Cognition Decline

Start date: December 15, 2019
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate whether perioperative probiotics can reduce the incidence of postoperative cognitive dysfunction and postoperative delirium.

NCT ID: NCT03745040 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Liposomal Bupivacaine in One-level Instrumented Posterior Spinal Fusion

Start date: January 26, 2019
Phase: Phase 4
Study type: Interventional

This study will describe postoperative pain management for spine surgery patients receiving liposomal bupivacaine (Exparel®) compared to patients not receiving the drug.

NCT ID: NCT03198273 Recruiting - Clinical trials for Lumbar Disc Herniation

The Efficacy of Clinical Pilates Exercises on Individuals With Lumbar Disc Herniation

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

The aim of the study is to determine the effects of clinical Pilates Exercises on the level of pain, functional status, flexibility, static and dynamic endurance of the truncus muscles and quality of life in patients with lumbar disc herniation.

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: NCT03002207 Recruiting - Clinical trials for Lumbar Disc Herniation

Repairing the Defect of Intervertebral Disc With Autologous BMSC and Gelatin Sponge After Microendoscopic Discectomy for Lumbar Disc Herniation

Start date: October 2016
Phase: N/A
Study type: Interventional

In this prospective study the investigators seek to evaluate clinical outcomes after repairing the defect of intervertebral disc with autologous BMSC/gelatin sponge during microendoscopic discectomy for participants of lumbar disc herniation.

NCT ID: NCT02110186 Recruiting - Clinical trials for Lumbar Disc Herniation

Lumbar Intervertebral Disc Herniation

LIDH
Start date: July 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to compare safety and outcomes of the following treatments of lumbar disc herniation: (1) discectomy with posterior dynamic stabilization with those of (2) discectomy alone or (3) discectomy with internal fixation and fusion. Discectomy with posterior dynamic stabilization is proposed as the most effective treatment to improve range of motion, and to be similarly effective to discectomy alone and discectomy with internal fixation and fusion for other functional outcomes after surgery.

NCT ID: NCT01363830 Recruiting - Clinical trials for Lumbar Disc Herniation

Short Versus Long Post-Operative Restrictions Following Lumbar Discectomy

Start date: August 2009
Phase: N/A
Study type: Interventional

Post-operative restrictions following lumbar discectomy is a controversial topic. While the most widely accepted protocol restricts bending, lifting, and twisting for four to six weeks following discectomy, a number of studies support an early return to full activity without restriction. Since the goal of discectomy is to promptly provide pain relief and a return to a fully active lifestyle, perhaps post-operative restrictions are more hindering than beneficial. Hypothesis: Post-operative restrictions following lumbar discectomy do not influence reherniation rate. Specific Aim 1: To compare the reherniation rates between the 6-weeks of restriction and the 2-weeks of restriction groups. Specific Aim 2: To determine the return to full activity and return to work dates of both the 6-weeks of restriction and 2-weeks of restriction groups. Specific Aim 3: To assess the health outcomes of both the 6-weeks of restriction and 2-weeks of restriction groups.