Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Can a smart gadget keep you out of the hospital after surgery?

NCT ID NCT04068584

Knowledge-focused Sponsor: Centre Hospitalier Universitaire de Nīmes Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a device called SMART ANGEL, which tracks heart rate, blood pressure, oxygen levels, and symptoms like pain and nausea at home, could reduce unplanned hospital visits, doctor calls, or extra prescriptions after major or intermediate outpatient surgery. Over 1,200 adults participated. The goal was to see if active home monitoring improves the quality of follow-up care.

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

1,260 people

The number who actually took part.

Started

Feb 2020

Finished

Nov 2024

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 to 80 years

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: * The patient must have given their free and informed consent and signed the consent form * The patient must be a member or beneficiary of a health insurance plan * The patient is undergoing ambulatory surgery for: * in orthopedics: shoulder (arthroscopy, abutment, prosthesis), hip (prosthesis, arthrolysis), knee (osteotomy, ligamentoplasty), ankle (prosthesis, ligamentoplasty) foot (hallux valgus); removal of major or multi-site equipment; * digestive (cholecystectomy, hernia repair, partial gastrectomy, colectomy, cleaning); * in gynecology (hysterectomy, oophorectomy, mastectomy, quadrantectomy, dissection, cystoplasty, sphincter); * in urology (total or partial resection of the prostate); * ENT (thyroidectomy, tonsillectomy); * Neurosurgery (herniated disc); * Vascular (stripping varix, creating fistula). * The patient has sufficient intellectual and cognitive capacity to use the devices * The patient must pass the test performed during the anesthesia consultation, namely: * open and connect the tablet, * activate the measurement of the blood pressure and the measurement of the oxygen saturation, * be connected to a 4G network Exclusion Criteria: * The subject is in a period of exclusion determined by a previous study * The subject refuses to sign the consent * It is impossible to give the subject informed information * The patient is under safeguard of justice or state guardianship * The patient is pregnant * The patient is undergoing emergency or minor surgery * Patient has a psychological class ASA 5 * Patient is non-eligible for ambulatory surgery for medical reasons (decompensated medical pathology) or social reasons according to the criteria defined by the société française anesthésie réanimation. Person lives alone or has a geographical distance from a hospital center\> 30 km (or\> 45 min by car). * Patient who doesn't classify for ambulatory surgery at time of discharge

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Ambulatory surgery are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Ambulatory surgery

Contacts and locations

Locations

  • CHU Lille

    Lille, 59000, France

  • CHU de Nimes

    Nîmes, 30029, France

  • CHU de Saint-Etienne

    Saint-Etienne, 42055, France

  • Centre Hospitalier Henri Duffaut

    Avignon, 84000, France

  • Centre hospitalier universitaire Amiens-Picardie

    Amiens, 80054, France

  • Clinique Bonnefon

    Alès, 30100, France

  • Clinique St Jean

    Saint-Jean-de-Védas, 34430, France

  • Hopital Nord

    Marseille, 13915, France

  • Hôpital Lapeyronie

    Montpellier, 34090, France

  • Hôpital Privé les Bonnettes

    Arras, 62000, France

  • Institut Mutualiste Montsouris

    Paris, 75674, France

  • Polyclinique Grand Sud

    Nîmes, 30900, France

More trials for these conditions

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