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Comparison of the Effectiveness of Two Postoperative Stabilization Protocols Sling Versus Standard Rehabilitation Exercises Without Sling on Clinical and Functional Outcomes in Patients With Rotator Cuff Tears Undergoing Arthroscopic Repair: A Randomized Clinical Trial

Comparison of the Effectiveness of Two Postoperative Stabilization Protocols Sling Versus Standard Rehabilitation Exercises Without Sling on Clinical and Functional Outcomes in Patients With Rotator Cuff Tears Undergoing Arthroscopic Repair: A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250630066302N1
Enrollment
100
Registered
2025-08-19
Start date
2025-09-06
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: orthopedics. Condition 2: orthopedics. Disorder of ligament, shoulder Rotator cuff tear or rupture, not specified as traumatic

Interventions

Intervention 1: Control group: Use of sling (In the control group, patients are required to use a sling for 4 weeks after surgery. Other parts of the postoperative physiotherapy protocol will be simil

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Adults (40 to 70 years old) with a complete rotator cuff tear measuring less than 3 cm with mild to moderate retraction (confirmed by MRI) Performing arthroscopic repair with the single-row technique Ability to participate in rehabilitation sessions and one-, three-, and six-month follow-ups

Exclusion criteria

Exclusion criteria: Large or massive rotator cuff tears (more than 3 centimeters) Presence of concomitant complications such as shoulder fracture, nerve damage, or rotator cuff arthropathy History of previous shoulder surgery or uncontrolled chronic diseases (diabetes, rheumatological diseases) Non-adherence to the protocol related to the control group (use of sling) or the intervention group (not using the sling as much as possible) or withdrawal from the study

Design outcomes

Primary

MeasureTime frame
Range of motion / functional outcomes / pain. Timepoint: 1, 2, 3 and 6 month. Method of measurement: Goniometry / DASH / SST / VAS.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hosein Khajavi Rad

Mashhad University of Medical Sciences

m.h.khajavi.rad@gmail.com+98 51 3841 2081

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026