Clinical Trials Directory

Trials / Completed

CompletedNCT02756598

Stress, Anxiety and Type A Personality and Analgesics

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

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Aarhus University Hospital · Academic / Other
Sex
Age
16 Years – 90 Years
Healthy volunteers
Not accepted

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).

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGSufentanil Ibolus dose of sufentanil 1 microgram/kg
DRUGSufentanil IIbolus dose of sufentanil 0.5 microgram/kg
DRUGPropofol IContinued dose of propofol 0.03 mg/kg/min
DRUGPropofol IIContinued dose of propofol 0.06 mg/kg/min

Timeline

Start date
2015-01-01
Primary completion
2018-01-01
Completion
2018-06-30
First posted
2016-04-29
Last updated
2019-07-10

Source: ClinicalTrials.gov record NCT02756598. Inclusion in this directory is not an endorsement.