Evaluation of short-term and mid-term results of using a cardiopulmonary pump in coronary artery bypass graft surgery

Phase 4

• Conditions: coronary artery disease.; Atherosclerotic heart disease of native coronary artery; I25.1

• Registration Number: IRCT20190120042428N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 November 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 272

Inclusion Criteria

patients with 3 vessels coronary artery disease
Candidates for coronary artery bypass graft surgery

Exclusion Criteria

require emergency operation
combined valve surgery
history of cardiac surgeries
patients with cardiogenic shock
patients with preoperative Intra-aortic balloon pump
patients with single or two vessel disease
patients with contraindication to off-pump CABG
history of renal failure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Major adverse cardiovascular events (MACE). Timepoint: 1, 3, 6, 12 months after surgery and then every 6 months until the end of the study. Method of measurement: The occurrence and type of major adverse cardiovascular events will be recorded during routine visits after surgery (at 1, 3, 6, and 12 month intervals) and at other intervals by telephone follow-up.