Evaluation of the effect of vitamin D before percutaneous coronary intervention in the prevention of cardiovascular complications
- Conditions
- Condition 1: Major adverse cardiovascular events. Condition 2: Precutaneous coronary intervention. Condition 3: Unstable angina.Abnormal result of cardiovascular function study, unspecifiedPresence of coronary angioplasty implant and graftAtherosclerotic heart disease of native coronary artery with unstable angina pectorisR94.30Z95.5I25.110
- Registration Number
- IRCT20210228050528N1
- Lead Sponsor
- Zanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 76
Patients with unstable angina who are candidates for PCI
Patients with deficient serum levels of vitamin D
Previous history of myocardial infarction
Previous history of revascularization therapy interventions
Patients with a previous history of CABG
Patients with failed PCI
Simultaneous involvement of valvular disorders
Take vitamin D, calcium or omega-3 supplements in the last 3 months
Patients with hypercalcemia, nephrolithiasis, sarcoidosis, malabsorption syndromes
Chronic underlying diseases such as liver, kidney or rheumatic disorders
Pregnancy and lactation
Having malignancies
History of receiving corticosteroids or immunosuppressants in the last 6 months
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of myocardial infarction cases. Timepoint: 3 and 6 months later. Method of measurement: ECG and echocardiography.;Number of revascularization cases in re hospitalization. Timepoint: 3 and 6 months later. Method of measurement: ECG and echocardiography.
- Secondary Outcome Measures
Name Time Method Readmission rate. Timepoint: 3 and 6 months later. Method of measurement: ECG and echocardiography.;Mortality rate. Timepoint: 3 and 6 months later. Method of measurement: In-person and telephone follow-up.;Cardiac function. Timepoint: 3 and 6 months later. Method of measurement: In-person follow-up.