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Stress, Anxiety and Type A Personality and Analgesics — SATA-1  

Postoperative; Dysfunction Following Cardiac Surgery Clinical Trial

Official title:
Stress, Anxiety and Type A Personality and Analgesics. Impact on Induction Time and Consumption of Analgesics During Cardiac Surgery

Clinical Trial Summary

Patients scheduled for elective cardiac surgery are preoperative evaluated using different personality type, stress and anxiety tests.

Patient are randomized to receive the investigators' standard moderate dose sufentanil (bolus 1microgram/kg and propofol 0.03 mg/kg/min) or low dose sufentanil (bolus 0.5 microgram/kg and propofol 0.06 mg/kg/min).

Clinical Trial Description

Patients randomized and the type of induction informed to the anaesthetist 30 minutes before surgery.

Patients are monitored before induction of anesthesia. Propofol is started on the randomized infusion rate. Sufentanil bolus are given according to randomization. BIS level is followed. Time to reach BIS < 50 is monitored. BIS after 30, 60 and 90 minutes are registered. Lowest BIS during surgery are registered. Total amounts of sufentanil and propofol recorded. ;

Study Design

Related Conditions & MeSH terms

  • Postoperative; Dysfunction Following Cardiac Surgery
Clinical Trial Details
NCT number NCT02756598
Study type Interventional
Source Aarhus University Hospital
Contact
Status Completed
Phase Phase 4
Start date January 2015
Completion date June 30, 2018
View Details
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