TerminatedNot Applicable

Automated Anesthesia Guided by the Conox Monitor for Surgery

Stopped: Modification of the device

France62 participantsStarted 2018-07-02

Plain-language summary

This study compares automated administration of propofol and remifentanil versus manual administration during general anesthesia for a surgery. The closed-loop coadministration of propofol and remifentanil is guided by qCon and qNox indexes from the Conox monitor.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Scheduled surgery for at least one hour * Consent for participation * Affiliation to the social security system Exclusion Criteria: * Pregnant or breastfeeding women * Patients for which Conox monitor should not be used * Allergies to propofol or remifentanil

What they're measuring

Adequate sedation

Timeframe: Start of general anesthesia maintenance, i.e. qCon below 60 for 30 consecutive seconds for the first time, until the end of propofol et remifentanil infusion

Trial details

NCT IDNCT03540875

SponsorCMC Ambroise Paré

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-02-18

View on ClinicalTrials.gov More Anesthesia, General trials