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Supra-spinatus Rehabilitation Program Comparison

Prospective Randomized Study Comparing 3 Post-operative Rehabilitation Programs After Arthroscopic Supra-spinatus Tendon Repair

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01467336
Enrollment
229
Registered
2011-11-08
Start date
2012-01-09
Completion date
2020-02-29
Last updated
2025-11-24

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

Conditions

Rotator Cuff Tear

Brief summary

Through a prospective randomized study the aims of this study is to analyze the impact of 3 types of rehabilitation protocols on the Optimization of the post-operative clinical and anatomic healing of the rotator cuff. After an arthroscopic repair of a stage 1 or 2 supra-spinatus tendon rupture, patients will be included in 3 groups (98 patients per group): * strict immobilization for 6 weeks then active rehabilitation, * or 3 weeks of immobilization then 3 weeks of passive motion before active rehabilitation, * or immediate passive motion for 6 weeks and then active rehabilitation. Patients will be evaluated clinically at 6 weeks, 3 months, 6 months and 1 year and an arthro-CT will be performed at 1 year. The investigators will evaluate: constant score and rate of tendon healing.

Interventions

PROCEDUREArthroscopic rotator cuff repair

Arthroscopic rotator cuff repair for all groups

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female between 40 and 65 years old * non-retracted supra-spinatus tendon tear-pre-operative clinical examination and ct * scan-arthroscopic single-row tendon repair

Exclusion criteria

* patient with a stiff shoulder * previous surgery of the shoulder * stage 3 or 4 fatty infiltration * insufficient repair of the cuff

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026