Clinical Trials Directory

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

TypeNameDescription
PROCEDUREArthroscopic rotator cuff repairArthroscopic 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.