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Lumbar Degenerative Disc Disease clinical trials

View clinical trials related to Lumbar Degenerative Disc Disease.

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NCT ID: NCT02139527 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

CARES Lumbar Artificial Disc Registry

Start date: May 2007
Phase: Phase 4
Study type: Observational [Patient Registry]

The purpose of the registry is to assess outcomes following treatment with lumbar total disc replacement (TDR) in patients outside the clinical trial setting.

NCT ID: NCT02070484 Terminated - Clinical trials for Musculoskeletal Diseases

Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the effect and safety of NuCel to DBX on patients undergoing posteriolateral lumbar spinal fusions for degenerative disc disease.

NCT ID: NCT01689922 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

The Effectiveness of Anti-Gravity Treadmill Training

Start date: June 2012
Phase: N/A
Study type: Observational

The primary objective of this study is to compare the effectiveness of standard for our practice postoperative physical therapy (PT) program to a PT program that incorporates lower body positive pressure (LBPP) treadmill training for the patients after lumbar discectomy and fusion surgeries.

NCT ID: NCT01294007 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

Radiographic Analysis Using PureGen Versus Autologous Bone in Posterolateral Fusion (PLF)

Start date: February 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the rate and quality of fusion of PureGen Osteoprogenitor Cell Allograft, compared to autograft bone in instrumented posterolateral fusion (PLF) procedures.

NCT ID: NCT01293981 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

Radiographic and Clinical Outcomes of PureGen in Posterior Lumbar (PLIF) and Transforaminal Interbody Fusion (TLIF)

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to assess the safety and efficacy of PureGen Osteoprogenitor Cell Allograft in patients undergoing Posterior Lumbar or Transforaminal Interbody Fusion.

NCT ID: NCT00878579 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

Percutaneous Dynamic Stabilization (PDS) System Versus Fusion for Treating Degenerative Disc Disease

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

The objective of this study is to evaluate the safety and effectiveness of the PDS System compared to the surgical control of posterolateral fusion with autograft and pedicle screw fixation for the treatment of one or two levels from L3-S1 to relieve back pain associated with degenerative disc disease.

NCT ID: NCT00744861 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

Ultrasound as Adjunct Therapy for Increasing Fusion Success After Lumbar Surgery

EXO-SPINE
Start date: September 2008
Phase: N/A
Study type: Interventional

Adjunct therapy for increasing posterolateral fusion success following single level posterior instrumented lumbar surgery.

NCT ID: NCT00640029 Terminated - Kyphosis Clinical Trials

Evaluation of the Prosthetic Disc Replacement

EVA
Start date: February 2008
Phase: N/A
Study type: Interventional

Until now, arthrodesis (intervertebral fusion) is the formal treatment for the lumbar and cervical degenerative disc disease : arthrodesis has been the standard surgical treatment for the patients when nonsurgical management has failed. However , it has shown out some drawbacks : pseudoarthrosis may appear in the short term, and junctional degeneration in the long term. The replacement of the intervertebral disc by a prosthesis (arthroplasty) has been since a few years a major alternative therapeutic to the arthrodesis.: it demonstrates great functional results and less post-interventional complications. It is indicated to restore a normal function of the spine (motion is kept)and to avoid deterioration of the adjacent spinal segments over the long time. In this clinical study, we will distinguish the cervical discal pathology and the lumbar discal pathology. The purpose of this study is to analyze the results of the arthroplasty in terms of functional effects, quality of life, anatomical results and economical results.

NCT ID: NCT00456378 Terminated - Clinical trials for Lumbar Degenerative Disc Disease

Study of the Safety and Effectiveness of DIAMâ„¢ Spinal Stabilization System Versus Conservative Care

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

The purpose of this study is to establish the safety and effectiveness of the DIAMâ„¢ Spinal Stabilization System in the treatment of moderate single-level lumbar degenerative disc disease.