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Search / Trial NCT05691374

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

Launched by UNIVERSITY HOSPITAL, BASEL, SWITZERLAND · Jan 10, 2023

Trial Information

Current as of July 12, 2025

Recruiting

Keywords

Shear Wave Elastography (Swe) Rotator Cuff Muscle Biceps Muscle Deltoid Muscle Trapezius Muscle Functional Outcome Biomechanical Outcome Biceps Tendon Infraspinatus Muscle (Isp) Teres Minor Muscle (Tm) Subscapularis Muscle (Ssc) Supraspinatus Muscle (Ssp)

ClinConnect Summary

This clinical trial is studying the outcomes of patients who have undergone arthroscopic rotator cuff repair (ARCR) surgery. Specifically, researchers want to see how well the tendons and muscles in the shoulder have healed over a period of 2 to 5 years after surgery. They will use a special ultrasound technique called shear-wave elastography (SWE) to measure the elasticity and strength of these tissues, comparing them to the healthy side of the shoulder.

To be eligible for this study, participants should have had ARCR surgery between 2015 and 2020 for specific types of rotator cuff tears. They should also be able to understand the study information and provide their consent. Participants can expect to undergo physical examinations and answer questions about their recovery. Remember, this trial is open to all genders and is currently recruiting participants aged 65 to 74. If you have had prior shoulder surgery, infections, or certain other conditions, you may not qualify for this study.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • year of surgery between 2015 and 2020
  • * ARCR surgery in cases of:
  • Partial or complete supraspinatus (SSP) tear
  • Partial or complete supraspinatus (ISP) tear
  • Partial or complete subscapularis (SSC) tear
  • Combined SSP, ISP and SSC tear
  • with or without biceps tenodesis during same procedure
  • able to understand the content of the patient information / consent form and give consent to take part in the study
  • Exclusion Criteria:
  • revision surgery (prior repair of the rotator cuff in the same shoulder)
  • postoperative infections
  • patients with a language barrier hindering questionnaire completion (either in German, French, Italian or English)
  • legal incompetence
  • not eligible for Ultrasound (BMI \>35, persistent frozen shoulder)
  • Prior surgery or injury of the contralateral shoulder

About University Hospital, Basel, Switzerland

The University Hospital Basel, Switzerland, is a leading academic medical center renowned for its commitment to cutting-edge research and innovative patient care. As a prominent clinical trial sponsor, the hospital leverages its extensive expertise and state-of-the-art facilities to advance medical knowledge and therapeutic options across various disciplines. With a collaborative approach that integrates clinical practice and scientific inquiry, the University Hospital Basel fosters an environment conducive to rigorous clinical trials, ensuring the highest standards of safety and efficacy. Its strategic focus on patient-centered research aims to translate scientific discoveries into tangible health solutions, benefiting both local and global communities.

Locations

Basel, , Switzerland

Patients applied

0 patients applied

Trial Officials

Andreas Müller, Prof. Dr. med.

Study Director

University Hospital Basel, Department of Orthopaedic and Trauma surgery

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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