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Comparison of the effect of intravenous ketorolac and paracetamol on pai

Phase 2
Recruiting
Conditions
Coronary artery bypass graft.
Registration Number
IRCT20180909040979N4
Lead Sponsor
Ahvaz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Age between 30 and 70 years
Candidate for coronary artery bypass graft

Exclusion Criteria

Gastrointestinal Disease
Kidney disease
Liver disease
EF<30%
Off pump surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postoperative pain control. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: VAS.;Arterial oxygen saturation drop. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: Yes or no.;Blood pressure changes. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: Three groups: mild to moderate.;Chest tube discharge. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: The volume of discharge.
Secondary Outcome Measures
NameTimeMethod
Arrhythmia. Timepoint: 0, 6, 12 and 24 hours after exteubation. Method of measurement: monitoring.;Duration of ventilator dependence. Timepoint: 0, 6, 12 and 24 hours after exteubation. Method of measurement: Duration of respiratory support.
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