Clinical Trials Directory

Trials / Completed

CompletedNCT03445494

Shoulder Abduction Brace Against Normal Sling After Arthroscopical Rotator Cuff Suture.

Shoulder Abduction Brace Against Normal Sling After Arthroscopical Rotator Cuff Suture: a Randomized Monocentric Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
108 (actual)
Sponsor
Christian Candrian · Academic / Other
Sex
All
Age
18 Years – 72 Years
Healthy volunteers
Not accepted

Summary

The patient undergoes arthroscopic surgery to treat rotator cuff injury. At the end of the surgery, the patient will be randomized into group A (brace) or group B (normal sling). Both groups will be also treated according to standard of care with physiotherapy and progressive introduction of movements.

Detailed description

The patient undergoes arthroscopic surgery to treat rotator cuff injury. At the end of the surgery, the patient will be randomized into group A (brace) or group B (normal sling). Both groups will then perform only passive movements according to pain for the first 6 weeks supported by the physiotherapy, according to standard therapy. The following six weeks passive movements will be associated with active movements . No brace nor normal sling will be used anymore. Patients are in study for 6 months. During this period quality of life and pain questionnaires are submitted to the patients and a MRI will be done at the end of the study.

Conditions

Interventions

TypeNameDescription
PROCEDUREBraceA brace to be weared according to protocol
PROCEDURENormal slingA normal sling to be weared according to protocol

Timeline

Start date
2018-01-10
Primary completion
2023-07-11
Completion
2023-07-11
First posted
2018-02-26
Last updated
2023-09-07

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03445494. Inclusion in this directory is not an endorsement.