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Herniated Disc clinical trials

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NCT ID: NCT01204008 Recruiting - Herniated Disc Clinical Trials

Conservative Versus Aggressive Discectomy for Primary Disc Herniation With Radiculopathy

Start date: September 2009
Phase: Phase 4
Study type: Interventional

Summary: This is a prospective randomize study to compare conservative and aggressive discectomy for treatment of disc herniation with radiculopathy. Study hypothesis: The investigators believe that conservative discectomy could preserve a higher disc space and has a better long-term outcomes.

NCT ID: NCT01014520 Recruiting - Clinical trials for Intervertebral Disc Displacement

Efficacy of Gabapentin or Amitriptyline to Reduce Postoperative Pain After Lumbar Laminectomy and Diskectomy

Start date: May 2009
Phase: Phase 2
Study type: Interventional

The hypothesis of this study is that Gabapentin or Amitriptyline has no role in preemptive analgesia to reduce postoperative pain after lumbar diskectomies.

NCT ID: NCT00974623 Terminated - Clinical trials for Degenerative Disc Disease

Bone Graft Materials Observational Registry

APPROACH-001
Start date: September 2009
Phase: N/A
Study type: Observational

A multi-center, prospective, observational patient registry to collect information on the clinical outcomes and "real world" use of approved and commercially available bone graft substitutes, autograft and allograft.

NCT ID: NCT00908375 Completed - Spinal Stenosis Clinical Trials

Efficacy of Pregabalin in Patients With Radicular Pain

Start date: May 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate whether pregabalin is effective in reducing the pain in patients who present with radicular pain due to a herniated disc, spinal stenosis or failed back surgery syndrome.

NCT ID: NCT00585923 Terminated - Radiculopathy Clinical Trials

Slotted Hole Versus Fixed Hole C-Tek

Start date: April 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the fusion rates between the EBI, LLC C-Tekā„¢ Anterior Cervical Plate, Slotted Hole Design versus the Fixed Hole Design.

NCT ID: NCT00405041 Completed - Herniated Disc Clinical Trials

Randomized Controlled Study to Assess the Efficacy of a Dietary Ingredient in Patients With Herniated Lumbar Disc Compression

Start date: November 2006
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of the study is to evaluate the efficacy of a neuroprotective dietary supplement in patients suffering from herniated lumbar disc causing nerve root compression.

NCT ID: NCT00300898 Withdrawn - Herniated Disc Clinical Trials

Radiofrequency Nucleoplasty vs Percutaneous Nucleotomy vs Decompression Catheter in Lumbar Disc Herniation

Start date: July 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to learn which of three minimally invasive procedures is the most effective for treatment of contained lumbar disc herniation.

NCT ID: NCT00269503 Terminated - Sciatica Clinical Trials

Chiropractic Prone Distraction for Lower Back Pain

Start date: March 2006
Phase: N/A
Study type: Interventional

Back pain is a major cause of disability in the United States. The lifetime prevalence of low back pain is estimated at 60-90%. Back pain has conservatively been estimated to involve total direct and indirect costs of over $25 billion annually in lost wages, treatment, and related issues. These losses clearly extend to the active duty population cared for by military health care facilities. Chiropractic medicine is characterized by the use of a number of physical manipulations and mobilization techniques, which can be used singly or in combination to treat a variety of medical conditions. Although basic clinical practice guidelines for Chiropractic have been developed, few studies have rigorously compared techniques and their outcomes for specific conditions. Fewer still have sought to correlate treatment modality with both anatomical effect and clinical outcome. Throughout the military, Chiropractic care is available only to active duty personnel and only at a limited number of medical treatment facilities. At National Naval Medical Center, it is a well-established treatment option, where the full array of techniques is employed, primarily for painful conditions, and most often for back pain. This study seeks to clarify the mechanisms of action and efficacy of one specific treatment option, prone distraction, for the relief of subacute sciatica due to radiographically confirmed herniated disc, and to compare it to side-posture manipulation and standard medical management. Prone lumbar distraction utilizes a specialized table with motorized continual motion distraction. This table has multiple mechanical articulations that can be used to place patients in a wide variety of positions. Patients being treated with continuous motion distraction are placed prone with the table positioned for maximum comfort and centralization of symptoms. Side posture manipulation is a widely practiced, standard chiropractic technique, which has been shown to provide considerable clinical improvement for patients with sciatica. Low- grade oscillatory stresses are performed within the physiological range of normal joint motion. The hip, pelvis and lumbar spine are rotated forward with manual pressure while a counter rotation of the chest and thoracic spine is applied.

NCT ID: NCT00124774 Completed - Herniated Disc Clinical Trials

Nucleoplasty for Contained Herniated Lumbar Discs

Start date: November 2004
Phase: Phase 3
Study type: Interventional

This is a prospective randomised double blind comparison trial. Fifty patients will be included, 25 in the nucleoplasty treatment group, 25 in the control group. The nucleoplasty group will undergo the nucleoplasty treatment. Control group will undergo a sham treatment. Both groups will undergo a standardised post-operative care program. The study hypothesis is that nucleoplasty will lead to earlier pain reduction as compared with the sham treatment.

NCT ID: NCT00107055 Active, not recruiting - Sciatica Clinical Trials

Study of REN-1654 in Patients With Sciatica Pain

Start date: December 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to gain initial safety and efficacy data on the experimental agent REN-1654 in patients with pain that radiates down the leg(s), and is typical of sciatica (lumbosacral radiculopathy). These patients will usually have a herniated disc that is causing compression on the nerves coming out of the spinal column.