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Which recovery plan works best after shoulder surgery?

NCT ID NCT06808269

Knowledge-focused Sponsor: Clinique Victor Hugo 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at two different approaches to follow-up care after shoulder surgery. One group gets structured homecare support through a service called Vivalto Dom, while the other manages recovery on their own with a local nurse. Researchers will track pain, comfort, and complications in 210 patients to find out which method leads to better outcomes.

What this could mean

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

What this could lead to
If successful, this could identify the best way to manage recovery after shoulder surgery, leading to better pain control and fewer complications.
What could go wrong
This is an observational study comparing existing care pathways, not testing a new treatment. Results may not apply to all hospitals or surgeries.

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 210 people

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

Started

May 2025

Expected to finish

Aug 2026

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: * Patient eligible for one of the following 4 types of surgery: Simple non-repair arthroscopic surgery (acromion, calcification), arthroscopic repair surgery (cuff, DAS, bankart), open surgery without prosthesis (ligamentoplasty, bone block), open surgery with prosthesis (inverted prosthesis, anatomic prosthesis, etc.). Exclusion Criteria: * Patients with one or more communication disorders. * Pregnant or breast-feeding patients * Patients not covered by a social security scheme * Refusal to participate in research * Patients unable to understand or give informed consent * Patients under guardianship, deprived of liberty or under court protection * Patients with past or present drug addiction * Patients with neuropathy * Patients with cognitive disorders * Patients with chronic illnesses or inflammatory pathologies leading to chronic pain.

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Conditions

The condition(s) this trial relates to.

Pain Shoulder Injuries

As listed by the trial registrant

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

Shoulder injury

How to take part

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

  1. The places running it

    2 sites. 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

  • Centre hospitalier privé Saint-Grégoire

    RECRUITING

    Saint-Grégoire, 35760, France

  • Clinique Victor Hugo

    RECRUITING

    Paris, 75116, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.