Clinical Trials Logo

Rotator Cuff Syndrome clinical trials

View clinical trials related to Rotator Cuff Syndrome.

Filter by:
  • Completed  
  • Page 1 ·  Next »

NCT ID: NCT05863806 Completed - Clinical trials for Rotator Cuff Syndrome

Mulligan Mobilization vs Transverse Friction Massage in Rotator Cuff Syndrome

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The aim of this research is to determine the Effects of Mulligan Mobilization and Transverse Friction Massage in Rotator Cuff Syndrome. Randomized clinical trials will be done at Northwest General Hospital, Peshawar. The sample size is 42. The subjects were divided in two groups, with 21 subjects in Group A and 21 in Group B. Study duration was of 6 months. Sampling technique applied was Non probability Purposive Sampling technique. Both males and females of aged 30-70 years with rotator cuff syndrome from grade (0-3) were included. Tools used in the study are Visual Analogue Scale (VAS), Goniometer, and DASH (Disabilities of the Arm, Shoulder and Hand) questionnaire. Data was analyzed through SPSS 23.

NCT ID: NCT05584345 Completed - Clinical trials for Rotator Cuff Syndrome

Investigation of the Effect of Respiratory Exercises on Pain and Functionality in Individuals With Rotator Cuff Syndrome

Start date: October 30, 2022
Phase: N/A
Study type: Interventional

As it causes pain and disability in individuals with rotator cuff lesions, which is one of the most common causes of shoulder pain, it affects performance in activities of daily living. Shoulder pain significantly affects the quality of life of individuals. The aim of conventional treatment in Rotator Cuff injuries is to reduce the inflammation in the area and to enable the shoulder to perform its normal functions. Conventional treatment is to restore muscle balance in the shoulder area. Muscle balance is achieved by strengthening the teres minor, infraspinatus, and subscapularis, which are also the humeral head depressors, and by strengthening the serratus anterior, levator scapula. For strengthening, the shoulder must have a full range of motion. In our study, stretching exercises, cold pack, Ultrasound, TENS, wand, and Codman exercises, which are classical physiotherapy methods, will be applied to all three groups. There are also studies in the literature investigating the effects of traditional physiotherapy methods on individuals with shoulder Rotator Cuff syndrome. The benefits of breathing exercises on pain, shoulder joint range of motion, and balance have all been researched in the literature. Increased diaphragm activity also guarantees that posture and body positions are maintained healthily. Diaphragm activity generally alters how an individual perceives pain. Diaphragmatic breathing is a therapeutic approach for musculoskeletal disorders.

NCT ID: NCT05561452 Completed - Shoulder Pain Clinical Trials

The Efficacy of PRP Injection in the Treatment of Rotator Cuff Syndrome

PRP
Start date: September 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the efficacy of single PRP injection compared with placebo and multiple PRP injections on pain, quality of life, shoulder function and muscle strength in the treatment of patients who have tendinopathy and/or partial tear in the rotator cuff.

NCT ID: NCT04716855 Completed - Clinical trials for Rotator Cuff Syndrome

Evaluation of Functional Status, Physical Activity and Quality of Life in Patients With Rotator Cuff Syndrome

Start date: March 25, 2015
Phase:
Study type: Observational [Patient Registry]

Pain is one of the most important factors affecting the quality of life. The quality of life of patients with pain and restricted shoulder movements can be affected in patients with Rotator Cuff Syndrome (RCS).

NCT ID: NCT02655848 Completed - Clinical trials for Rotator Cuff Syndrome

Tenotomy or Tenodesis of Long Head Biceps in Arthroscopic Rotator Cuff Repair

BITE
Start date: July 2012
Phase: N/A
Study type: Interventional

During arthroscopic rotator cuff (infraspinatus/supraspinatus) repair, biceps tendon lesions are frequently encountered. However, the most optimal treatment of the diseased long head of the biceps (LHB) tendon during rotator cuff repair remains a topic of debate: tenotomy or tenodesis. The hypothesis is that there is no difference in functional outcome between LHB tenotomy and LHB tenodesis when performed in adjunct to arthroscopic rotator cuff repair.

NCT ID: NCT02495818 Completed - Clinical trials for Rotator Cuff Syndrome

Suprascapular Nerve Block Guided by Ultrasound

Start date: June 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the effect of suprascapular nerve block guided by ultrasound combined with home exercises compared with placebo. Pain intensity, function, pressure pain threshold and goniometry were designed to be assessed in all patients.

NCT ID: NCT02493660 Completed - Clinical trials for Rotator Cuff Syndrome

A Pivotal Study to Assess the InSpaceā„¢ Device for Treatment of Full Thickness Massive Rotator Cuff Tears

Start date: June 26, 2015
Phase: N/A
Study type: Interventional

A pivotal study to assess the safety and effectiveness of the InSpaceā„¢ device implantation in comparison to surgical partial repair of full thickness Massive Rotator Cuff Tear (MRCT).

NCT ID: NCT01996904 Completed - Clinical trials for Rotator Cuff Syndrome

Prospective Randomized Comparative Study of Outcome of Subscapularis Tear

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study was to report actual percentage of subscapularis tear in concomitant with supraspinatus tendon tear (with or without infraspinatus tear) and investigate the amount of contribution of subscapularis repair as to the outcome of whole rotator cuff repair in terms of its clinical and radiologic aspects.

NCT ID: NCT01987973 Completed - Rotator Cuff Injury Clinical Trials

Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone

Start date: February 2015
Phase: N/A
Study type: Interventional

The investigators hypothesize that the use of an allograft adjuvant to partial repair will lead to improved shoulder outcome measure scores compared to partial repair alone in massive rotator cuff tears.

NCT ID: NCT01702233 Completed - Clinical trials for Rotator Cuff Syndrome

TRARO (Traumeel® S in Rotator Cuff Syndrome)-Study

TRARO
Start date: April 2013
Phase: Phase 3
Study type: Interventional

To evaluate functional, clinical, and subjective parameters in patients with rotator cuff syndrome and bursitis treated with Traumeel® S injections versus corticosteroid injections and versus placebo. 160 patients are planned to be randomised (i.e., 64 patients per active treatment group and 32 patients in the placebo group) in 9 investigator sites in Germany, Belgium and Spain. Finally 176 patients have been randomized (73 Traumeel, 67 Fortecortin and 36 Placebo) and 175 of them received at least one dosage of treatment