Value of Capsular Repair for Latarjet

Prospective, Multicenter, Randomized Single-blind Study on the Interest of Capsular Repair in the Latarjet Operation

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05978362

Acronym

CAP-LATARJET

Enrollment

Registered

2023-08-07

Start date

2023-10-11

Completion date

2037-12-01

Last updated

2026-05-13

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

Conditions

Shoulder Pain

Brief summary

The purpose of the study is to evaluate the occurrence of osteoarthritis (YES/NO) by radiography.

Detailed description

This is a prospective, comparative, longitudinal, randomized, single-blind, multicenter study. This study will validate preliminary results on a technique associating capsular repair with abutment according to Latarjet in the treatment of shoulder instabilities. It may help reduce the risk of osteoarthritis and thus allow patients to maintain a healthy, stable and painless shoulder for longer.

Interventions

PROCEDURELatarjet technique

Realization of a stop according to Latarjet

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Subject)

Masking description

randomized single-blind study

Intervention model description

prospective, comparative, longitudinal, randomized single-blind study

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Patient, male or female, over the age of 18 * Patient with shoulder instability with risk factors for recurrence (ISIS score \> 3), requiring surgical stabilization by abutment * Affiliated patient or beneficiary of a social security scheme * Patient having been informed and having given his free, informed and written consent.

Exclusion criteria

* Patient with history of surgery for instability of the same shoulder * Patient presenting contraindications to the realization of a postoperative scanner * Patient whose physical and/or psychological health is severely impaired, which according to the investigator may affect the compliance of the study participant * Patient participating in another clinical research or in a period of exclusion from another research still in progress at the time of inclusion * Protected patient: adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision * Pregnant, breastfeeding or parturient woman * Patient hospitalized without consent.

Design outcomes

Primary

Measure	Time frame	Description
occurrence of osteoarthritis	10 years	Change from occurrence of osteoarthritis (YES/NO) on X-ray at 5 and 10 years, compared to inclusion X-ray using the Samilson-Prieto classification.

Countries

France

Contacts

CONTACTGeoffroy NOURISSAT, MD

gnourissat@wanadoo.fr768513650

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026