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Rotator Cuff Tears clinical trials

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NCT ID: NCT04774965 Not yet recruiting - Surgery Clinical Trials

The Effects of SlumberCurve™ Following Rotator Cuff Surgery: A Randomized Control Trial

Start date: June 30, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effects of a novel sleep aid known as SlumberCurve™, which serves as an adjustable form of a wedge pillow, on sleep quality and pain management following rotator cuff repair. The researchers hypothesize that SlumberCurve™ will significantly improve sleep quality and reduce night-time pain.

NCT ID: NCT04686968 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Microfracture Combined With Suture Bridge Technique Versus Greenhouse Technique in Treating of Rotator Cuff Injuries

Start date: July 2021
Phase: N/A
Study type: Interventional

Several biological augmentation procedures have recently been suggested to enhance tendon healing after Arthroscopic rotator cuff repair, such as marrow-stimulating technique with microfractures of the greater tuberosity. The purpose of this study was to introduce a new technique, "greenhouse technique", and to compare the clinical outcomes with microfracture combined with suture bridge technique.

NCT ID: NCT04681937 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Comparison of Hyaluronic Acid, PRP and Steroid Injections in Partial Rotator Cuff Tears: A Prospective Randomized Study

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

There are many conservative treatment options available for partial rotator cuff tears. However, the superiority of a certain type of injection could not be demonstrated with the available data. Our aim is to compare the effectiveness of steroid, hyaluronic acid, prp and placebo (normal saline) injections in partial rotator cuff tears by applying the same physical therapy protocol after injection.

NCT ID: NCT04587037 Not yet recruiting - Rotator Cuff Tears Clinical Trials

A Clinical Study Comparing Superior Capsule Reconstruction Using Different Graft for Irreparable Rotator Cuff Tear

Start date: October 2020
Phase: N/A
Study type: Interventional

Biomechanical and clinical success of the superior capsule reconstruction (SCR) using fascia lata (FL) grafts has been reported in treating irreparable rotator cuff tear. Human dermal (HD) allograft has been used successfully for SCRs; however, the clinical comparative study between FL and HD have not been reported.

NCT ID: NCT04584476 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Superior Capsular Reconstruction Versus. Partial Repair for Irreparable Rotator Cuff Tears

Start date: October 2020
Phase: N/A
Study type: Interventional

Rotator cuff tear is one of the common injuries that cause shoulder pain in the elderly. After the rotator cuff tendon is injured, repairing the torn rotator cuff tendon through arthroscopic surgery is an effective treatment that is currently widely used. In the rotator cuff injury, irreparable rotator cuff injury is a difficult point in treatment, especially for patients with a long injury time, the obvious shrinkage of the injured tendon, muscle atrophy and steatosis may occur, all of which lead to the poor quality of the rotator cuff tendon needed to be repaired , Poor healing ability, seriously affecting the shoulder joint function and daily life of these patients. For this part of patients, arthroscopic partial repair of torn rotator cuffs is one of the commonly used methods. In addition, in recent years, superior capsular reconstruction has been gradually applied to the clinic and has achieved good clinical effects, but there are no controlled studies to compare Clinical effect of partial repair and superior capsular reconstruction on irreparable rotator cuff injury.

NCT ID: NCT04538001 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Safety and Efficacy of Rotator Cuff Function Restoration Balloon in Irreparable Rotator Cuff Tear

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

This study is a prospective, multicenter, randomized, controlled clinical study aiming to evaluate the safety and efficacy of the rotator cuff function restoration balloon in patients with irreparable rotator cuff tear compared to partial repair of the rotator cuff.

NCT ID: NCT04364542 Not yet recruiting - Postoperative Pain Clinical Trials

Suprascapular Nerve Block Efficacy for Shoulder Surgery

Start date: May 10, 2020
Phase: N/A
Study type: Interventional

This study evaluates the analgesia induced by suprascapular nerve block in comparison to interscalene nerve block in arthroscopic rotator cuff repairs. The experimental and the control group will receive the suprascapular nerve block and interscalene nerve block, respectively.

NCT ID: NCT04047745 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Post-operative Exparel Study Following Rotator Cuff Repair

Start date: September 2019
Phase: N/A
Study type: Interventional

The primary purpose of this study is to determine if the postoperative oral narcotics consumption in patients receiving liposomal bupivacaine (LB) interscalene brachial plexus nerve block (ISBPB) is different than the narcotics consumption receiving traditional bupivacaine ISBPB for arthroscopic rotator cuff repair analgesia.