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Clinical Trials/ISRCTN15105737
ISRCTN15105737
Completed
Not Applicable

Remifentanil versus sufentanil regimen for intensive care unit (ICU) postoperative sedation after coronary artery bypass graft surgery: a prospective, randomised and double-blinded study

Saint Luc University Clinic (Cliniques Universitaires Saint Luc) (Belgium)0 sites40 target enrollmentAugust 8, 2008
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ConditionsPostoperative sedation of an elective coronary artery bypass graft surgery (CABG)Circulatory SystemOther and unspecified disorders of circulatory system

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative sedation of an elective coronary artery bypass graft surgery (CABG)
Sponsor
Saint Luc University Clinic (Cliniques Universitaires Saint Luc) (Belgium)
Enrollment
40
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 8, 2008
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Saint Luc University Clinic (Cliniques Universitaires Saint Luc) (Belgium)

Eligibility Criteria

Inclusion Criteria

  • •1\. Both males and females, age \>18 years
  • •2\. Patients scheduled for elective CABG with cardiopulmonary bypass (CBP)
  • •3\. Signed informed consent

Exclusion Criteria

  • •1\. Simultaneous valve surgery or any other combined surgery
  • •2\. Poor preoperative cardiac function (ejection fraction \<30%, severe congestive heart failure)
  • •3\. Liver or renal disorders
  • •4\. Chronic respiratory diseases
  • •5\. Alcohol or drugs abuse and neurological or psychiatric conditions that might impair pain evaluation
  • •Postoperative exclusion criteria:
  • •6\. Situations where the administration of the anaesthetic regimen was maintained after the fourth postoperative hour

Outcomes

Primary Outcomes

Not specified

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