Comparison of the effect of three medications on clinical symptoms of patients undergoing open heart surgery

Phase 3

Recruiting

• Conditions: Coronary artery bypass graft surgery.; Atherosclerosis of coronary artery bypass graft(s), unspecified, with unspecified angina pectoris; I25.709

• Registration Number: IRCT20120215009014N391
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 26 May 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Age of 40 to 70 years,
Candidate for coronary artery bypass graft surgery,

Exclusion Criteria

Diabetes,
Requires emergency coronary artery bypass graft surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Heart rate. Timepoint: One minute before induction of anesthesia and at 1, 2, 5 and 10 minutes after intubation. Method of measurement: Using monitoring machine.;Systolic blood pressure. Timepoint: One minute before induction of anesthesia and at 1, 2, 5 and 10 minutes after intubation. Method of measurement: Using monitoring machine.;Mean arterial blood pressure. Timepoint: One minute before induction of anesthesia and at 1, 2, 5 and 10 minutes after intubation. Method of measurement: Using monitoring machine.;Electrocardiographic changes. Timepoint: One minute before induction of anesthesia and at 1, 2, 5 and 10 minutes after intubation. Method of measurement: Using monitoring machine.;Diastolic blood pressure. Timepoint: One minute before induction of anesthesia and at 1, 2, 5 and 10 minutes after intubation. Method of measurement: Using monitoring machine.