The comparative effect of two methods of rehabilitation in patients after arthroscopic shoulder rotator cuff tendon repair.

Not Applicable

• Conditions: Complete rotator cuff tear or rupture not specified as traumatic.; Injury of muscle(s) and tendon(s) of the rotator cuff of shoulder; S46.0

• Registration Number: IRCT20201010048978N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 May 2021

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Patients aged 30-75 years
The origin of the rupture should be progressive damage
The size of the rupture is small and medium (= <3 cm)
Patients with complete rupture of the rotator-cuff muscles except subscapularis
Since this operation is usually performed in conjunction with other restorative procedures such as subacromial decompression and distal clavicle resection; to increase the generalizability to the community in this study, patients can be accompanied by these operations.

Exclusion Criteria

Any complication in the shoulder girdle area such as arthritis of the shoulder joint or destructive joint disease as well as SLAP and Bankart surgery
Traumatic tears that result from direct trauma or injury and tears larger than 3 cm
Existence of neurological disorders such as disorders Neurological with sensory and muscular problems
Radicular pain from the neck or chest (Increased/developed shoulder symptoms with active or inactive neck movement)
History of fracture, dislocation or shoulder complex surgery
History of RSD
History of recurrent dislocation or joint instability Shoulder in the last 3 months
Symptoms of preoperative capsular adhesion characterized by a loss of more than 50% of inactive range of motion compared to the non-involved side in at least two shoulder movements

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain intensity. Timepoint: Before the start of the treatment plan/after the completion of the treatment plan. Method of measurement: Visual Analogue Scale (VAS).