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Pain control after coronary artery bypass grafting surgery (CABG)

Phase 2
Completed
Conditions
Coronary artery disease.
Atherosclerotic heart disease
Registration Number
IRCT2015012814359N3
Lead Sponsor
Vice chancellor for research of Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
68
Inclusion Criteria

Patients aged 30-65 years;Three vessels disease (3VD)
Exclusion criteria:Patients not extubated after 8 hours;Patients requiring reoperation for bleeding ;Patients with advanced heart failure (requiring high-dose postoperative inotropic or need to put intra-aortic balloon pump (IABP)

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Every 2 hours for 12 hours and then every 4 hours to 24 hours. Method of measurement: Using verbal pain score (VPS).0-10.
Secondary Outcome Measures
NameTimeMethod
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