Clinical Trials Logo

Intervertebral Disc Degeneration clinical trials

View clinical trials related to Intervertebral Disc Degeneration.

Filter by:

NCT ID: NCT02440074 Withdrawn - Clinical trials for Degenerative Disc Disease

Lumbar Degenerative Disc Disease Treatment With Bone Marrow Autologous Mesenchymal Stem Cells (MSV)

MSV-DISC
Start date: June 2011
Phase: Phase 1/Phase 2
Study type: Interventional

This trial pretends to validate for clinical use a bioengineered product composed of mesenchymal stem cells produced by the Instituto de Biologia y Genetica Molecular (IBGM), Valladolid (MSV, which have already been approved by the Spanish Regulatory Agency for three previous clinical trials) and a cross-linked matrix of autologous plasma patented by The Blood and Tissue Bank of Asturias (WO2008/ 119855) for bone maxillary cysts refilling. These two groups collaborate in the present project with the team of Maxillofacial Surgery of the Hospital Universitario del Río Hortega, who leads the clinical trial and deals with the medical aspects. The proposed trial is based on positive results obtained in previous animal studies performed by the present multidisciplinary team. A phase I / II clinical trial with 10 patients suffering from bone cysts in the maxillofacial region is proposed. Autologous mesenchymal stem cells isolated from a bone marrow sample will be seeded in the autologous plasma matrix and cultivated for 3 weeks. At this time, the cyst will be removed by surgery and the cavity filled with the protein matrix containing the mesenchymal cells. Follow up tests will be conducted at 3 weeks, 3 and 6 months following the evolution of the cavity by panoramic radiography and computerized tomography scan.

NCT ID: NCT02371122 Withdrawn - Clinical trials for Failed Back Surgery Syndrome

Spinal Cord Stimulation (SCS) Therapy Study

Start date: June 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of different spinal cord stimulation settings in the treatment of leg pain. Subjects will receive a randomized order of four different programmed stimulation settings for 3 weeks each followed by a fifth and final setting.

NCT ID: NCT02170558 Withdrawn - Clinical trials for Degenerative Disc Disease

Enhanced Metal Reduction Techniques for Definitive CT Scanning to Assess Spinal Fusion With TM-Ardis

Start date: June 2014
Phase:
Study type: Observational

To determine if the subject metal reduction software helps to better visualize bone interphase and fusion reliability. Assess whether the appropriate procedural modification facilitates clearer images when implanted with a trabecular metal spinal implant

NCT ID: NCT01643681 Withdrawn - Clinical trials for Lumbar Intervertebral Disc Degeneration

Autologous Adipose Tissue Derived Mesenchymal Stem Cells Transplantation in Patient With Lumbar Intervertebral Disc Degeneration

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

The purpose of this study is to investigate the efficacy and safety of autologous transplantation of Adipose Tissue derived Mesenchymal stem cells (MSCs) in patient with lumbar intervertebral disc degeneration.

NCT ID: NCT01616719 Withdrawn - Clinical trials for Cervical Radiculopathy

Evaluation of DTRAX Graft in Patients With Cervical Degenerative Disc Disease

Start date: May 2012
Phase: N/A
Study type: Interventional

DTRAX Graft is used to relieve nerve pressure in the neck in order to provide relief for Cervical Degenerative Disc Disease. This study is being conducted to determine the effectiveness of the graft, and to find out whether or not it provides better results or faster healing than traditional ways of performing surgery for Cervical Degenerative Disc Disease.

NCT ID: NCT01016314 Withdrawn - Clinical trials for Degenerative Disc Disease

Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusion (ALIF)

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

This is a multi-center, prospective randomized clinical study to evaluate the clinical outcome of subjects with degenerative disc disease (DDD) treated with ALIF and supplemental posterior fixation using ASPEN Spinous Process System compared to pedicle screw instrumentation.

NCT ID: NCT00810212 Withdrawn - Clinical trials for Degenerative Disc Disease

Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate safety and preliminary efficacy of Neofusetm in subjects with a diagnosis of degenerative disc disease (DDD) in 1 or 2 adjacent vertebral levels between L1 and S1 and undergoing posterolateral lumbar fusion.