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Active clinical trials for "Intervertebral Disc Degeneration"

Results 41-50 of 415

The Synergy Disc To Anterior Cervical Discectomy and Fusion

Cervical Degenerative Disc Disease

A multicenter, prospective, non-randomized, historically controlled study. Demonstrate the Synergy Disc is at least as safe and effective as conventional anterior cervical discectomy and fusion (ACDF) to treat cervical degenerative disc disease (DDD) in subjects who are symptomatic at only one level from C3 to C7 that are unresponsive to conservative management. Patients will be evaluated preoperatively, at the time of surgery, and at 6 weeks, 3, 6, 12, and 24 months after surgery. Follow-up will continue annually until the last patient reaches 24-month follow-up. The primary analysis will occur at 24 months.

Active47 enrollment criteria

Study of Posterior Cervical Stabilization System (PCSS) as Part of Circumferential Fusion to Treat...

Degenerative Disc Disease

This study will evaluate the safety and effectiveness of a device called "Posterior Cervical Stabilization System or PCSS" when used along with posterior cervical fusion (PCF) in combination with anterior cervical discectomy and fusion (ACDF) in the treatment of multi-level cervical degenerative disease.

Active34 enrollment criteria

KUR-113 Bone Graft Versus Local Autograft for the Treatment of Single-level Transforaminal Lumbar...

Degenerative Disc DiseaseSpinal Fusion

The purpose of this study is to evaluate the safety and efficacy of KUR-113 Bone Graft (TGplPTH1-34 in fibrin) compared to local autograft for the treatment of Degenerative Disk Disease (DDD).

Active44 enrollment criteria

VIA Disc NP Pilot for Patients With Symptomatic Degenerated Discs

Degenerative Disc DiseaseLow Back Pain1 more

VIA Disc NP is an allograph intended to supplement the nucleus pulposus tissue in degenerated intervertebral discs.

Active48 enrollment criteria

Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE...

C-CURVE Cervical Interbody Cage2 more

This study includes one type of product named C-CURVE which is a Stand-alone Cervical Interbody Cage. This product is available in two materials: PEEK and Titanium. The C-Curve Cervical Interbody Devices is one single implant used for insertion between two adjacent vertebrae (cervical spine). C-Curve has been designed to restore and/or maintain adequate interbody height, and thus help stabilize one or more cervical levels while fusion occurs. This system has also as objectives to increase of the quality of life, decrease patient's pain and decrease a potential dysphagia (clinical performances). This system must only be used in the cervical spine. This post-market clinical follow-up (PMCF) study aims to confirm the acceptable benefits/risk profile of the device for the patients and to fill essential requirements to maintain the CE mark through a clinical evaluation.

Active14 enrollment criteria

TLIF Osteo3 ZP Putty Study (Also Known as the TOP Fusion Study)

Degenerative Disc DiseaseDegenerative Spondylolisthesis1 more

In recent years there has been an increase in interest from surgeons in the use of synthetic bone graft substitutes to avoid the need of sourcing allograft or iliac crest autograft for use in spinal fusion procedures. This will be an open label, prospective, first in man, single-centre clinical study to evaluate the safety and performance of Osteo3 ZP Putty synthetic bone graft in TLIF procedures with instrumentation. Safety and performance data obtained in this clinical study will be used to estimate clinical success rates achieved with the use of Osteo3 ZP Putty synthetic bone graft in TLIF procedures. No comparative control group is intended. The study is expected to run for approximately three years with each subject being followed up for a two- year post-operative period. The target is to recruit approximately 17 subjects to this clinical study, allowing for some subject attrition to get 15 evaluable.

Active22 enrollment criteria

Safety, Tolerability, and Effectiveness of Intramuscular Injection of CELZ-201-DDT for the Treatment...

Chronic Low-back PainDegenerative Disc Disease

The brief purpose of this research study is to learn about the safety, tolerability, and efficacy of paraspinal intramuscular injection of CELZ-201-DDT in patients with chronic lower back pain.

Not yet recruiting24 enrollment criteria

Real World Data Collection and Analysis on the Anterior Cervical Spine Surgery

Cervical Disc Degeneration

This observational study aims to evaluate the efficacy and safety of anterior cervical spine surgery in patients with cervical degenerative disc disease

Recruiting8 enrollment criteria

Post-Market Clinical Follow-Up Study on the Safety and Performance of Ennovate® Cervical

Spine FractureDegenerative Disc Disease3 more

Multicenter Post market clinical follow-up Study on the Safety and Performance of Ennovate® Cervical - Prospective, pure data collection of all Ennovate Cervical patients in Total Indications

Recruiting5 enrollment criteria

Prospective Study of Thoracolumbar Spinal Fusion Graft

Lumbar Degenerative Disc Disease

This study is a single-center, prospective randomized clinical study intended to compare and evaluate the efficacy of subjects who are treated with bone marrow aspirate concentrate (BMAC) and allograft to iliac crest bone grafts (ICBG) during posterior lumbar/lumbosacral spinal fusion.

Active15 enrollment criteria
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