Trials / Terminated
TerminatedNCT01467336
Supra-spinatus Rehabilitation Program Comparison
Prospective Randomized Study Comparing 3 Post-operative Rehabilitation Programs After Arthroscopic Supra-spinatus Tendon Repair
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 229 (actual)
- Sponsor
- University Hospital, Strasbourg, France · Academic / Other
- Sex
- All
- Age
- 40 Years – 65 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Arthroscopic rotator cuff repair | Arthroscopic rotator cuff repair for all groups |
Timeline
- Start date
- 2012-01-09
- Primary completion
- 2020-02-01
- Completion
- 2020-02-01
- First posted
- 2011-11-08
- Last updated
- 2025-11-24
Locations
4 sites across 1 country: France
Source: ClinicalTrials.gov record NCT01467336. Inclusion in this directory is not an endorsement.