Clinical Trials Logo

Rotator Cuff Injuries clinical trials

View clinical trials related to Rotator Cuff Injuries.

Filter by:

NCT ID: NCT03648047 Terminated - Rotator Cuff Tear Clinical Trials

Digital Biofeedback System Versus Conventional Rehabilitation After Rotator Cuff Repair

Start date: November 11, 2018
Phase: N/A
Study type: Interventional

This study was designed to compare the clinical outcomes of a mixed home-based rehabilitation program after arthroscopic rotator cuff repair, incorporating face-to-face sessions as well as sessions performed with a novel digital kinematic biofeedback system against conventional in-person home-based rehabilitation, with the intent of reducing the need for face-to-face sessions. The investigators hypothesize that the clinical outcomes of such a program will be at least similar to those of conventional rehabilitation. Patients will be enrolled pre-operatively and then randomized into 2 groups: experimental group and conventional rehabilitation group. Both groups will perform a 12 to 16-week rehabilitation program starting immediately after surgery. Outcomes will be measured at baseline, 8 and 12 weeks. In patients where a decision is made to extend the program to 16 weeks, another assessment will be made at this point.

NCT ID: NCT03617562 Recruiting - Rotator Cuff Tear Clinical Trials

Superior Capsular Reconstruction vs. Partial Repair for Massive Rotator Cuff Tears

SCR
Start date: July 18, 2018
Phase: N/A
Study type: Interventional

Little evidence exists to guide treatment in patients with massive irreparable rotator cuff tears (MRCTS). Arthroscopic partial rotator cuff repair (PRCR) has the longest record of use. The new technique of superior capsular reconstruction (SCR) has more recently been described. Despite high enthusiasm for this technique, its effectiveness, cost and safety profile have not been established. The long-term goal of this study is to perform a multicenter randomized control trial to evaluate the effectiveness of SCR compared to PRCR in patients with MRCTS. The current study is a pilot required to support the development of an expanded formal clinical trial.

NCT ID: NCT03617107 Active, not recruiting - Rotator Cuff Tear Clinical Trials

Reverse Total Shoulder Arthroplasty: A Data Analysis on Patients Undergoing Reverse Total Shoulder Arthroplasty

rTSA
Start date: December 15, 2017
Phase:
Study type: Observational

The purpose of this study is to evaluate reverse total shoulder arthroplasty patients preoperative objective measurements and operative objective measurements to determine if there is any effect to postoperative outcomes. Patients who were 18 years old or greater at the time of surgery were followed clinically and radiographically to determine best practice and optimal treatment and technique, risk and rate of complication, and postoperative outcomes.

NCT ID: NCT03616340 Not yet recruiting - Rotator Cuff Tear Clinical Trials

Efficacy of Intra-articular NSAID Versus Corticosteroid in the Treatment of Shoulder and Knee Conditions: A Randomized, Double-Blind, Prospective Study

Start date: August 2018
Phase: Phase 3
Study type: Interventional

The proposed study will compare the efficacy of Triamcinolone versus Ketorolac for intra-articular injection of the knee and shoulder

NCT ID: NCT03609164 Completed - Rotator Cuff Tear Clinical Trials

Does the Suture-spanning Augmentation of Single-row Repair in Massive Rotator Cuff Tear Reduce the Retear Rate?

Start date: May 1, 2015
Phase: N/A
Study type: Interventional

There are several associated structural changes when dealing with massive rotator cuff repair, which include tendon retraction and fragility, muscle atrophy and fatty infiltration, as well as osteoporosis over the tendon insertion. Those changes may lead to difficult in applying double-row repair, suture cutting through the tendon, too much tension over the repair and loosening or pull-out of anchors, which may results in poor tendon-bone healing and subsequent high re-tear rate. Therefore decreasing the tension over the repair site may increase the healing over tendon bone junction as well as decrease the risk of anchors loosening. A suture-spanning augmentation with two set of suture loops passing over musculotendinous junction medially and fixed with anchor at the lateral cortical wall may solve the problem. In order to define the clinical benefit of this adjuvant procedure, a prospective randomized control study is designed to compare the adjunctive reinforce suture with the single-row simple suture repair in massive rotator cuff tear. Around sixty patients were randomized divided into two groups. The study group was used adjunctive reinforce suture repair technique, which was one lateral cortical anchor holding 2 separated set of transverse looping sutures over the medial musculotendinous junction in addition to single row repair, while the control group was used single row repair technique in simple stitch fashion. All patients will have clinical evaluation in pain (VAS score) and functional recovery (ASES and UCLA score) as well as MRI image for the tendon integrity. If the suture-spanning augmentation of single-row repair can yield an improved healing rate and fewer complications, massive rotator cuff tear should be repaired earlier in order to prevent the late development of irreparable tear.

NCT ID: NCT03597490 Terminated - Clinical trials for Partial Thickness Rotator Cuff Tear

Multimodal Physical Therapy With Exercise in Partial-thickness Rotator Cuff Tears

Start date: July 1, 2018
Phase:
Study type: Observational

The aim of this study is to investigate the early stage effectiveness of multimodal physical therapy with exercise in the conservative treatment of partial thickness rotator cuff tears.

NCT ID: NCT03577379 Completed - Rotator Cuff Tear Clinical Trials

Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The goal of this study is to assess whether undergoing surgical repair of the rotator cuff with the additional intervention of whole blood fibrin clot will improve rotator cuff vascularization at the bone-tendon interface repair site and patient outcomes compared to those who do not receive the whole blood fibrin clot intervention.

NCT ID: NCT03573765 Completed - Osteoarthritis Clinical Trials

Epidemiology and Outcomes of Upper Limb Surgery: Analysis of Routine Data

Start date: April 6, 1998
Phase:
Study type: Observational

Surgery is a common treatment type for damaged joints, tendons and nerves in the upper limb where conservative measures are inappropriate or have failed. These conditions are common and result in significant levels of pain and functional disability. The investigators are conducting a broad ranging study of variation in the provision of surgical treatment and factors affecting outcomes after surgical treatment of upper limb conditions. This will be a population-based study of all patients undergoing surgical treatment funded by the National Health Service (NHS) of England over a nineteen-year period. This study will help to understand the factors associated with a poor outcome following surgery, which can be shared with patients considering treatment options. The investigators will also document current and future health service burden associated with commonly performed surgical procedures including complications and repeat operations.

NCT ID: NCT03567954 Terminated - Rotator Cuff Tear Clinical Trials

The Accuracy of Ultrasound in Detecting Rotator Cuff Tears in Proximal Humerus Fracture Patients

Start date: June 22, 2018
Phase:
Study type: Observational

The aim of this study is to determine the diagnostic accuracy of ultrasonography (US) in detecting full-thickness (a lesion that extends through both the bursal and articular part of the tendon) rotator cuff tear in patients who have sustained a proximal humerus fracture, using operative examination as the golden standard.

NCT ID: NCT03567109 Completed - Clinical trials for Carpal Tunnel Syndrome

Body Schema Alterations in Musculoskeletal Disorders : Effect of Laterality

Schem-TMS
Start date: July 13, 2018
Phase:
Study type: Observational [Patient Registry]

This study assess ocular movements in a hand laterality judgment task in a population of musculoskeletal disorders. Reaction time, error rate and visual strategy are compared between musculoskeletal disorders and healthy patients, and between the different locations of the disorder.