Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07154641

Latissimus Dorsi Tendon Transfer vs. Superior Capsular Reconstruction in Massive Rotator Cuff Tears

Led by Konstantopoulio-Patission General Hospital of Nea Ionia · Updated on 2025-09-04

44

Participants Needed

1

Research Sites

199 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare the results of two surgical operations for the treatment of massive rotator cuff tears: latissimus dorsi tendon transfer (LDT) and superior capsular reconstruction (SCR). The main question it wants to answer is which of the two operations provides better functional results, as measured by two patient-reported questionaires: the American Shoulder and Elbow Surgeons (ASES) score and the Constant-Murley score. The patients will be randomly assigned to one of two groups according to the surgery they will undergo (LDT or SCR). They will be examined clinically and asked to fill the questionaires before the surgery, at 6 weeks and at 3, 6, 12 and 24 months after surgery.

CONDITIONS

Official Title

Latissimus Dorsi Tendon Transfer vs. Superior Capsular Reconstruction in Massive Rotator Cuff Tears

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 years or older
  • Diagnosis of massive rotator cuff tear confirmed by shoulder MRI
Not Eligible

You will not qualify if you...

  • Advanced glenohumeral arthritis (Hamada stage 3 or higher)
  • Deltoid muscle dysfunction
  • Irreparable subscapularis tendon tear
  • Presence of infection
  • Previous shoulder surgery
  • Shoulder stiffness

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

Konstantopouleio-Patision General Hospital of Nea Ionia

Athens, Attica, Greece, 14233

Actively Recruiting

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Research Team

D

Dimitrios V Papadopoulos, MD, PhD

CONTACT

A

Athanasios Kontogiannis, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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