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Stress, Anxiety and Type A Personality and Analgesics

NCT02756598 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2019-07-10

No results posted yet for this study

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).

Conditions

  • Postoperative; Dysfunction Following Cardiac Surgery

Interventions

DRUG

Sufentanil I

bolus dose of sufentanil 1 microgram/kg

DRUG

Sufentanil II

bolus dose of sufentanil 0.5 microgram/kg

DRUG

Propofol I

Continued dose of propofol 0.03 mg/kg/min

DRUG

Propofol II

Continued dose of propofol 0.06 mg/kg/min

Sponsors & Collaborators

  • Aarhus University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
90 Years
Sex
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-01-31
Primary Completion
2018-01-01
Completion
2018-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02756598 on ClinicalTrials.gov