Condition 1: Atrial fibrillation after CABG. Condition 2: Atrial fibrillation after CABG. Paroxysmal atrial fibrillation Unspecified complication of cardiac and vascular prosthetic device, implant and graft
Conditions
Interventions
Intervention 1: Intervention group: In group A 300000 IU of vit D (equivalent of 2 cc of 300000 IU vial) will be given to the patients 72 hours before the surgery. Intervention 2: Intervention group:
Sponsors
Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
45 Years to 80 Years
Inclusion criteria
Inclusion criteria: Patients who are condidated for elective CABG that have informed consent for joining to the study. All patients that duration of their surgery is less than 6 hours. Serum level of vit D less than 30 nanomol per litr
Exclusion criteria
Exclusion criteria: History of having arrhythmia and atrial fibrillation History of using antiarrhythmic drugs in class I and III or Digoxin History of having permanent or temporary heart pace maker History of atrioventricular block or bradycardia with less than 50 heart beat per minute History of severe kidney or pulmonary (pneumonia or chronic obstractive pulmonary disease ) or liver (cirrhosis or fulminant hepatitis) disease Non elective CABG Patients who need heart valve replacement surgery, in addition to CABG
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Frequency of post CABG atrial fibrillation. Timepoint: From the end of surgery untill 72 hours after surgery. Method of measurement: heart monitoring. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAlireza Kamali
Arak University of Medical Sciences
Outcome results
None listed