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Clinical Trials/IRCT201510314583N7
IRCT201510314583N7CompletedPhase 1

comparison the sedative effect of propofol and ketofol on patients undergoing coronary artery bypass graft (CABG) in intensive care unit (ICU)

Vice chancellor of Shahid Sadoughi university of medical sciences.0 sites45 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Sponsor
Enrollment
45

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
40 years to 60 years (—)
Sex
All

Inclusion Criteria

  • patients 40-60 years old with ASA 1,2 undergoing CABG in ICU in Afshar Hospital
  • Exclusion criteria: patients requiring inotropic drugs; patients with impaired renal tests; addicted patients ; ejection fraction <40%; patients requiring hospitalization in the ICU for more than 24 hours; patients with known psychiatric problems; patients with history of seizure

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice chancellor of Shahid Sadoughi university of medical sciences.

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