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Can an extra ligament repair make shoulder stabilization surgery more effective?

NCT ID NCT07756827

Disease control Sponsor: Clinique Générale dAnnecy Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 11, 2026 · Last updated Sep 11, 2026 · Updated 3 times

Summary

This trial is testing two surgical approaches for people with recurrent anterior shoulder instability (repeat dislocations). Both use the Latarjet procedure, where a piece of bone is moved to stabilize the joint. One group also gets an extra capsular repair using a nearby ligament, while the other does not. The study aims to see if adding this repair improves outcomes like stability, range of motion, and complications, and to gather preliminary data for a larger future trial.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Surgical procedure: open Latarjet with or without anterior capsuloplasty using the coracoacromial ligament
What this could lead to
If successful, this could help determine whether adding capsular repair to the Latarjet procedure improves shoulder stability and function, potentially guiding future surgical practice.
What could go wrong
This is a small pilot study, so results may not be definitive. Surgery carries risks like infection, nerve damage, or recurrence of instability, and the added capsuloplasty may not provide significant benefit.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 42 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2026

Expected to finish

Feb 2031

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Recurrent anterior shoulder instability with critical glenoid bone loss and a potential concomitant Hill-Sachs lesion requiring surgical management. * Patients must be able to provide written informed consent and be willing to adhere to the postoperative rehabilitation protocol and the scheduled follow-up. Exclusion Criteria: * History of bone stabilization procedures on the affected shoulder * Multidirectional shoulder instability * Full-thickness rotator cuff tear * Neuromuscular disorder affecting shoulder function and range of motion * Active infection, inflammatory arthritis, or tumor affecting the shoulder region * Patients unable or unwilling to participate in the study or to undergo follow-up assessments * Individuals deprived of liberty, in pre-trial detention, or under guardianship, curatorship, or judicial protection * Individuals undergoing psychiatric care * Individuals not affiliated with a social security scheme

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Conditions

The condition(s) this trial relates to.

Kinesiophobia

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Recurrent anterior shoulder instability

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Clinique Générale d'Annecy

    RECRUITING

    Annecy, 74000, France

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