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Recruiting

NCT Number: NCT07488039

Labroplasty in Cases of Anterior Shoulder Instability With Subcritical Glenoid Bone Loss

The goal of this clinical trial is to learn Labroplasty using the long head of biceps tendon works to patients with recurrent anterior shoulder instability with subcritical glenoid bone loss (<20%) and thinned or deficient anterior labrum .The main questions it aims to answer are:

Does Labroplasty using the long head of biceps improve the functional and radiological outcomes in patients with recurrent anterior shoulder instability with subcritical glenoid bone loss?

Participants will:

undergo arthroscopic labroplasty using the long head of biceps tendon Visit the clinic regularly for checkup and followup undergo MRI at 6 months to check radiological outcome

Recruiting

Interested in participating?

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Key information

Age range

16 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kasr El Aini Hospital

Cairo, Cairo Governorate, Egypt

Location status: Recruiting

Location contact

Sherif Walid Ibrahim, Assistant Lecturer

CONTACT

[email protected]

+201271377782 ext. 002

sherif Walid Ibrahim, Assistant Lecturer

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • patients with recurrent anterior shoulder instability with one or more events of anterior shoulder dislocation.
  • Franceschi types 2 and 3 labral defects
  • subcritical glenoid bone loss <20%
  • positive anterior shoulder apprehension

Exclusion criteria

  • Critical glenoid bones loss >20%
  • Franceschi type 1 labral defect
  • concomitant long head of biceps tendon pathology
  • multidirectional instability
  • prior arthroscopic shoulder stabilization surgery
  • concomitant proximal humeral fractures
  • concomitant Rotator cuff tears
  • skeletally immature patients
  • glenoid pathology
  • Shoulder arthritis
  • active infection

Treatment and study plan

Arthroscopic Labroplasty using long head of biceps tendon

Procedure

Arthroscopic All-inside labral reconstruction using the long head of biceps tendon

Primary outcomes

  1. Change in Modified Rowe score postoperative

    Time frame: Assessed preoperative , then at 6 months and 12 months postoperative

Secondary outcomes

  1. Constant shoulder score

    Time frame: assessed preoperative , then at 6 months and 12 months postopertive

Study contacts

Contact information is provided by the study sponsor or research team.

Sherif Walid Ibrahim, Assistant Lecturer

CONTACT

[email protected]

+201271377782 ext. 002

Sponsors and collaborators

Lead sponsor

Kasr El Aini Hospital

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Mar 23, 2026
Registry last updated
Mar 23, 2026

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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