IRCT20240527061915N1RecruitingPhase 3
Comparing the prophylactic effect of adding magnesium to Metoral in reducing atrial fibrillation after coronary artery bypass graft surgery
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Recruiting
- Enrollment
- 102
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 35 years to 75 years (—)
- Sex
- All
Inclusion Criteria
- •All CABG candidate patients referred to Amirul Mominin Arak Hospital
- •All patients candidates for elective operations
- •The age of patients between 35-75 years
- •All patients are candidates for CABG only
- •All patients who are operated with that pump
- •All patients with informed consent to participate in this study
- •The average duration of surgery is maximum 7 hours
- •All patients who do not have heart valve repair surgery with CABG
- •ASA?,? patients
- •Patients who are not allergic to Metoral-Magnesium
- •All patients who have acid-base disorders resistant to treatment before surgery
Exclusion Criteria
- •Patients who suffer cardio-respiratory arrest during surgery
- •Patients who do not agree to continue the study or cooperate
- •All CABG candidate patients who require valve repair during surgery
- •All patients who, after the induction of anesthesia, the surgeon decides to perform surgery with the pump OFF
- •All patients who have acid-base disorders resistant to treatment before surgery
Investigators
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