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Spinal Degeneration clinical trials

View clinical trials related to Spinal Degeneration.

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NCT ID: NCT04911283 Completed - Spinal Degeneration Clinical Trials

Brucella Serology and History of Brucellosis in Patients With Modic Changes Type 1

Start date: May 1, 2019
Phase:
Study type: Observational

Objective: This study aims to examine Brucella serology and history of brucellosis in patients with lumbar Modic changes (MCs) type 1, considering results from cross-sectional and case-control comparisons. Design: In comparative cross-sectional design, MCs type 1 patients (study group) and MCs type 2 patients (comparator group) were examined in terms of Brucella serology by using agglutination with Coombs test. In addition, in comparative case-control design, both of the MCs groups and age/sex-matched healthy controls were investigated for their medical history regarding brucellosis.

NCT ID: NCT04670536 Active, not recruiting - Spinal Deformity Clinical Trials

The Degen Study: Post-market Clinical Follow-up on the PASS LP, PASS Degen and PASS Tulip Systems (PASS DEGEN)

PASS DEGEN
Start date: May 17, 2018
Phase:
Study type: Observational

The purpose of this post-market clinical study is to evaluate the long-term safety and efficacy of the MEDICREA's systems PASS LP, PASS DEGEN, and PASS Tulip PRIME to treat degenerative diseases. This study is supporting the clinical evaluation report. From the standard-of-care perspective, the results of The Degen study are expected to contribute to a better understanding of expected safety and clinical outcomes from a short (intra- and peri-operative) to a medium-term follow-up (post-operatively).

NCT ID: NCT03898232 Completed - Clinical trials for Degenerative Disc Disease

Fibergraft Interbody Fusion Retrospective

FIFR
Start date: May 9, 2019
Phase:
Study type: Observational

A single center study of clinical and radiological outcomes in a retrospective cohort of patients treated with Lumbar Interbody Fusion augmented with Prosidyan Fibergraft for 1 or 2 level degenerative spinal disease by a single surgeon. Study Design: Retrospective chart review with prospective data collection.

NCT ID: NCT03632005 Recruiting - Spinal Cord Injury Clinical Trials

Negative Pressure Wound Therapy vs. Sterile Dressing for Patients Undergoing Thoracolumbar Spine Surgery

Start date: March 18, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of the Prevena™ System decreases the rate of subcutaneous seroma, superficial wound dehiscence and infection.

NCT ID: NCT01608854 Completed - Clinical trials for Surgical Wound Infection

Comparison of Antibiotic Protocols in Spine Patients With Postoperative Drains

Start date: November 2008
Phase: N/A
Study type: Observational

In spine surgery, postoperative spinal drains are often utilized to prevent fluid buildup around the spinal cord. The purpose of this study is to determine whether postoperative antibiotic treatment continued for the duration of time a drain is in place results in a lower infection rate than antibiotics given for only 24 hours postoperatively.