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Full Thickness Rotator Cuff Tear clinical trials

View clinical trials related to Full Thickness Rotator Cuff Tear.

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NCT ID: NCT04115644 Terminated - Clinical trials for Rotator Cuff Tendinitis

Effectiveness of Corticosteroid vs. Ketorolac Shoulder Injections: A Prospective Double-Blinded Randomized Trial

Start date: May 1, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the functional outcomes of patients with shoulder pathology treated with either ketorolac or corticosteroid injections, in a randomized double-blinded study. Investigators will compare the effectiveness of ketorolac compared to corticosteroid. Specific Aim 1: Hypothesis 1: Injection of the shoulder (in the subacromial space) with Ketorolac will be more effective than corticosteroid injection for the treatment of a variety of shoulder pathologies. The risks associated with this study primarily concern adverse reactions to the study drugs. The drugs used in this study are not narcotics or habit-forming but can have side effects. The patient's physician will screen for any heart, intestinal, or kidney disease or condition that would increase the chance for the patient to have an unwanted side effect.

NCT ID: NCT03339492 Terminated - Clinical trials for Full-thickness Rotator Cuff Tear

PEMF as Adjunctive Treatment Following Surgical Repair of Full Thickness Rotator Cuff Tears

RCStim
Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The primary objective of this study is to prospectively determine, at 12 months post-surgical repair of full thickness rotator cuff tears, the safety and efficacy of treating full thickness rotator cuff repairs with pulsed electromagnetic fields (PEMF). The hypothesis states that exposure to a pulsed electromagnetic field (PEMF) following surgical repair of a full thickness rotator cuff tendon tear reduces tendon re-tear rates. The strength of the shoulder muscles and the levels of pain in subjects after surgical repair of their rotator cuff adjunctively treated with an active PEMF device will also be measured.

NCT ID: NCT02208440 Terminated - Clinical trials for Full-thickness Rotator Cuff Tear

InSpaceā„¢ System in Comparison to Best Repair of Massive Rotator Cuff Tear.

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

This is a post-marketing study to further assess the safety and effectiveness of the InSpaceā„¢ device implantation in comparison to surgical repair of full thickness Massive Rotator Cuff Tear .