TerminatedNot Applicable

Automated Postoperative Sedation After Cardiac Surgery

Stopped: Modification of the device

France7 participantsStarted 2018-12-17

Plain-language summary

This study compares automated administration of propofol and remifentanil guided by the Bispectral index (BIS) versus manual administration for sedation after cardiac surgery.

Who can participate

Age range18 Years – 80 Years

SexALL

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

Inclusion Criteria: * Cardiac surgical procedure requiring postoperative sedation * Low operative risk : EuroSCORE 2 ≤ 5% * Consent for participation * Affiliation to the social security system Exclusion Criteria: * Pregnant or breastfeeding women * Neurological or muscular disorder * Pacemaker * Hypersensitivity to propofol or remifentanil * Communication difficulties or neuropsychiatric disorder

What they're measuring

Adequate sedation

Timeframe: 6 hours

Trial details

NCT IDNCT03517735

SponsorCMC Ambroise Paré

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-03-28

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