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Prophylactic effect of tranexamic acid capsule in controlling epistaxis

Phase 3
Conditions
Epistaxis.
Epistaxis
R04.0
Registration Number
IRCT20180425039418N7
Lead Sponsor
Zahedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Insensitivity to the drugs used in the study
Satisfaction to enter the study

Exclusion Criteria

Patients with seizure, arterial or venous thrombosis, leukemia, lymphoma, polycythemia vera, pregnant women
Patients who have taken anticoagulants, anti-platelets and even aspirin

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Patient satisfaction from treatment based on questionnaire. Timepoint: Every week from the start of treatment and up to one month after treatment. Method of measurement: questionnaire.
Secondary Outcome Measures
NameTimeMethod
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