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

Who should control your sedation during surgery? new study compares options

NCT ID NCT06451380

Symptom relief Sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at whether letting patients control their own sedation during arm surgery under regional anesthesia leads to higher satisfaction compared to having an anesthesiologist control it. 70 adults having upper limb orthopedic surgery were randomly assigned to either patient-controlled or anesthesiologist-controlled sedation with propofol. The main goal was to see which group reported better overall experience.

What this could mean

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

Active substance
propofol
What this could lead to
If it works, this could give patients more control over their sedation during surgery, potentially improving comfort and satisfaction.
What could go wrong
This is a small, completed trial with only 70 participants, so results may not apply to everyone. Patient-controlled sedation may not be suitable for all patients or procedures.

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

70 people

The number who actually took part.

Started

Oct 2024

Finished

Jan 2025

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: * Patients aged 18 and over; * Patients indicated for orthopedic surgery of the upper limb under anaesthesia requiring additional sedation; * Ability to use the patient-controlled sedation device; * Body Mass Index less than 40 kg/m²; * American Society of Anesthesiologists Class I to III; * Patient agreeing to study assessments and follow-up visits * Patient having been informed and agreeing to participate in the study by signing an informed consent form. Exclusion Criteria: * Contraindications to locoregional anesthesia (allergy, local infection, coagulation disorders); * Surgery of the upper limb not compatible with locoregional anesthesia (arthroplasty); * Patient unable to understand study information for linguistic, psychological or cognitive reasons linguistic, psychological or cognitive reasons ; * Patient pregnant or likely to be pregnant, of childbearing age, without effective contraception or breastfeeding ; * Patient participating in another clinical trial, or in a period of exclusion from another clinical trial; * Patient under legal protection, or deprived of liberty by judicial or administrative decision administrative ; * Patient not covered by a social security scheme.

Get updates

Get notified about this study

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

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

Conditions

The condition(s) this trial relates to.

musculoskeletal system disorder

As listed by the trial registrant

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

Orthopedic disorder

Contacts and locations

Locations

  • Clinique Jouvenet

    Paris, 75016, France

More trials for these conditions

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