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Evaluation of the effect of vitamin D before percutaneous coronary intervention in the prevention of cardiovascular complications

Phase 3
Conditions
Condition 1: Major adverse cardiovascular events. Condition 2: Precutaneous coronary intervention. Condition 3: Unstable angina.
Abnormal result of cardiovascular function study, unspecified
Presence of coronary angioplasty implant and graft
Atherosclerotic heart disease of native coronary artery with unstable angina pectoris
R94.30
Z95.5
I25.110
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
Inclusion Criteria

Patients with unstable angina who are candidates for PCI
Patients with deficient serum levels of vitamin D

Exclusion Criteria

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
NameTimeMethod
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
NameTimeMethod
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.
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