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Outcomes of Warfarin and Rivaroxaban (Xalerban) consumption in patients with Atrial fibrillatio

Phase 4
Recruiting
Conditions
Atrial fibrillation.
Chronic atrial fibrillation
I48.2
Registration Number
IRCT20170530034232N2
Lead Sponsor
Vice-Chancellor For Research and Technology of Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
330
Inclusion Criteria

Being over 50 years old
Patients with Atrial fibrillation
CHAD2S2 Vasc Score more than 1

Exclusion Criteria

Patient's dissatisfaction with the study
Wolff Parkinson White Syndrome
Allergic to any of the drugs Rivaroxaban (Xalerban) and warfarin
Abnormal Creatinine level
Thrombocytopenia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: All patients will be followed up by researchers every 15 days in the first month and then every month for 6 month. Method of measurement: Measurement of coagulation factors and hemoglobin level by blood test.
Secondary Outcome Measures
NameTimeMethod
Changes in liver's enzymes. Timepoint: All patients will be followed up by researchers every 15 days in the first month and then every month for 6 month. Method of measurement: Measurement of liver's enzymes (SGOT, SGPT) by blood test.
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