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

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT07488039

Enrollment

Registered

2026-03-23

Start date

2026-01-01

Completion date

2027-12-31

Last updated

2026-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent Anterior Shoulder Instability

Keywords

Labroplasty

Brief summary

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

Interventions

PROCEDUREArthroscopic Labroplasty using long head of biceps tendon

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

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Intervention model description

Single arm clinical trial

Eligibility

Sex/Gender

ALL

Age

16 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Change in Modified Rowe score postoperative	Assessed preoperative , then at 6 months and 12 months postoperative

Secondary

Measure	Time frame
Constant shoulder score	assessed preoperative , then at 6 months and 12 months postopertive

Countries

Egypt

Contacts

CONTACTSherif Walid Ibrahim, Assistant Lecturer

sherif_shibl@yahoo.com+201271377782

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026