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

NCT03445494 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 108

Last updated 2023-09-07

No results posted yet for this study

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.

Conditions

  • Supraspinatus Injury

Interventions

PROCEDURE

Brace

A brace to be weared according to protocol

PROCEDURE

Normal sling

A normal sling to be weared according to protocol

Sponsors & Collaborators

  • Clinical Trial Unit Ente Ospedaliero Cantonale

    collaborator OTHER

  • Christian Candrian

    lead OTHER

Principal Investigators

  • Christian Candrian, MD · EOC

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
72 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-10
Primary Completion
2023-07-11
Completion
2023-07-11

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03445494 on ClinicalTrials.gov