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Determination of optimal prophylactic dose of magnesium sulfate for prevention of atrial fibrillation after CABG surgery

Determination of optimal prophylactic dose of magnesium sulfate for prevention of atrial fibrillation after CABG surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201211124365N15
Enrollment
120
Registered
2012-12-15
Start date
2011-05-22
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial fibrillation. Atrial fibrillation and flutter

Interventions

Intervention 1: Intervention 1: 60 mg/Kg MgSO4 via cardioplegic solution during cross clamping. Intervention 2: Intervention 2: 80 mg/Kg MgSO4 via cardioplegic solution during cross clamping. Interven
Prevention
Intervention 1: 60 mg/Kg MgSO4 via cardioplegic solution during cross clamping
Intervention 2: 80 mg/Kg MgSO4 via cardioplegic solution during cross clamping
Intervention 3: 100mg/Kg MgSO4 via cardioplegic solution during cross clamping

Sponsors

Vice chancellor for research of Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: signing informed consent; candidate for elective CABG based on angiography; use of cardiopulmonary bypass (CBP) during surgery; no previous history of any cardiac dysrhythmias that is under treatment ( including AF); hemodynamic stability ( MAP>50, heart rate between 50-110); age between 35&75 years old. Exclusion criteria: history of heart failure (Ejection Fraction less than 30%); more than 4 grafts; renal failure ( serum creatinine >1.5 in two consecutive test); hepatic failure ( liver function tests more than 1.5 times of normal value); history of COPD; hyperthyroidism; serum PH 7.55; postoperative MI; second or third degree AV block; need for pacemaker after surgery; reoperation for any reason; history of pervious cardiac surgery; anti-arrhythmic drugs consumption (except beta blocker).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Atrial fibrillation. Timepoint: up to 3 days after operation. Method of measurement: ECG monitoring.

Secondary

MeasureTime frame
PH. Timepoint: Before Before trial, during the operation,1st day, 2nd day and 3th day after operation, during the operation,1st day, 2nd day and 3th day after operation. Method of measurement: Laboratory kit.;K. Timepoint: Before Before trial, during the operation,1st day, 2nd day and 3th day after operation, during the operation,1st day, 2nd day and 3th day after operation. Method of measurement: Laboratory kit - mEq/L.;Mg. Timepoint: Before Before trial, during the operation,1st day, 2nd day and 3th day after operation, during the operation,1st day, 2nd day and 3th day after operation. Method of measurement: Laboratory kit - mg/dl.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfshin Gholipour Baradari, MD

Mazandaran University of Medical Sciences

gholipourafshin@mazums.ac.ir; gholipourafshin@yahoo.com+98 15 1222 6262

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026