Actively Recruiting

Age: 18Years +
All Genders
NCT05691374

Evaluation of Functional and Biomechanical Outcome by Shear-wave Elastography in the Short to Intermediate Follow-up After Arthroscopic Rotator Cuff Repair

Led by University Hospital, Basel, Switzerland · Updated on 2025-05-20

75

Participants Needed

1

Research Sites

131 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Basel, Switzerland

Lead Sponsor

D

DePuy Synthes

Collaborating Sponsor

AI-Summary

What this Trial Is About

This exploratory project will evaluate the biomechanical and functional intermediate-term outcome (2 to 5 years) after arthroscopic rotator cuff repair (ARCR) with modern non-invasive ultrasound techniques (especially shear wave elastography (SWE)), standardized physical examinations and patient-reported outcomes. It is to evaluate the biomechanical properties of tendons and muscles of the rotator cuff, as well as the biceps muscle after ARCR and to compare elasticity and structural properties to the healthy contralateral side.

CONDITIONS

Official Title

Evaluation of Functional and Biomechanical Outcome by Shear-wave Elastography in the Short to Intermediate Follow-up After Arthroscopic Rotator Cuff Repair

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Year of surgery between 2015 and 2020
  • Arthroscopic rotator cuff repair surgery for partial or complete tear of supraspinatus (SSP), infraspinatus (ISP), or subscapularis (SSC) tendon
  • Surgery with or without biceps tenodesis during the same procedure
  • Able to understand patient information and provide consent to participate
Not Eligible

You will not qualify if you...

  • Revision surgery or prior rotator cuff repair in the same shoulder
  • Postoperative infections
  • Language barrier preventing questionnaire completion in German, French, Italian, or English
  • Legal incompetence
  • Not eligible for ultrasound due to BMI over 35 or persistent frozen shoulder
  • Prior surgery or injury of the opposite shoulder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospital Basel, Department of Orthopaedic and Trauma surgery

Basel, Switzerland, 4031

Actively Recruiting

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Research Team

D

Dominik M Bühler, Dr. med.

CONTACT

I

Ilona Ahlborn

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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