Could a simple checklist after anesthesia save lives?
NCT ID NCT03972423
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This trial investigates whether using a structured transmission checklist when patients arrive in the post-anesthesia care unit (PACU) can reduce the risk of dangerously low oxygen levels. About 560 adults recovering from anesthesia will be randomly assigned to standard handover or handover with the checklist. The main goal is to see if the checklist lowers the rate of oxygen desaturation below 90% for more than 15 seconds.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a transmission checklist for handover communication
- What this could lead to
- If effective, this simple checklist could become a standard tool to prevent breathing complications after surgery.
- What could go wrong
- This is a relatively small study testing a behavioral intervention, so results may not apply to all hospitals or patient groups.
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.
- Participants
-
560 people
The number who actually took part.
- Started
-
Feb 2019
- Finished
-
Jul 2020
- 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.
Who is studied
adult patients admitted to PACU
- 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 Hide 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: * Male or Female over 18 admitted to PACU * Patient having understood the aims and the methods of the research * Patient having expressed their consent to the use of their data. * Subject registered with or beneficiary of a social security scheme Exclusion Criteria: * Patient participating in another clinical study * Acute or chronic respiratory insufficiency preoperatively * Protected patient: adult under guardianship, tutorship or other legal protection, deprived of liberty by judicial or administrative decision * Pregnant or lactating women
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Anesthesia are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Les Franciscaines Clinic
Versailles, IDF, 78000, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Which monitor reads a Child's pain best during surgery?
- Propofol vs. inhaled anesthesia: which one spares your recovery?
- Can a dissolvable bone wax curb bleeding during spine fusion?
- Can a safer opioid choice stop Kids' Post-Surgery agitation?
- Can a different anesthesia approach tame inflammation after chest surgery?
- Which epidural technique best handles a cesarean emergency?