TerminatedNot Applicable

Postoperative Sedation After Cardiac Surgery

Stopped: Intermediate analysis

France19 participantsStarted 2015-05

Plain-language summary

This pilot study evaluates the effectiveness of a closed-loop administration of propofol and remifentanil guided by the bispectral index for short-term 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: * consent for participation * cardiac surgical procedure requiring postoperative sedation Exclusion Criteria: * pregnant women, * neurological or muscular disorder * high risk of revision surgery * patients having required a redo operation if the postoperative period of sedation was less than 2 hours

What they're measuring

Level of sedation

Timeframe: 6 hours

Trial details

NCT IDNCT02488486

SponsorHopital Foch

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2017-05

View on ClinicalTrials.gov More Surgery, Cardiac trials