Automated Postoperative Sedation After Cardiac Surgery

• Status: Terminated
• Trial end date: 2019-03-30
• Target enrollment: 0
• Participant gender: All

Summary

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

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: CMC Ambroise Paré
• Treatments: Propofol; Remifentanil

Criteria

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