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OpenTrials
Completed

NCT Number: NCT06394856

Comparison of Outcomes of Rotator Cuff Repair With a Modified Versus Classic Double-Row Suture -Bridge Techniques

rotator cuff tears are one of the most common shoulder issues , affecting 20.7% of the general population .

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Key information

Conditions

Rotator Cuff Tears Rotator Cuff Injuries Rupture Shoulder Injuries Tendon Injuries Wounds and Injuries

Age range

40 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

university Hospital

Sohag, 82511, Egypt

About this study

accompanied by shoulder pain and dysfunction

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • full-thickness supraspinatus
  • degenerative tears
  • age range 40 :65

Exclusion criteria

  • subscapularis tear
  • small and massive tears
  • traumatic tears
  • partial -thickness tear
  • revisioin surgery
  • glenohumeral arthretic changes and shoulder instability

Treatment and study plan

Rotator Cuff Repair With a Modified Versus Classic Double-Row Suture -Bridge Techniques

Procedure

rotator cuff tears with modified versus classic double row suture bridge

Primary outcomes

  1. retear rate

    Time frame: 3 years

    retear rate

Secondary outcomes

  1. time

    Time frame: 3 years

    duration of operation

Sponsors and collaborators

Lead sponsor

Sohag University

Other

Registry information

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
May 1, 2024
Registry last updated
Jun 13, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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