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effectiveness of local Tranexamic Acid on Epistaxis Control in patients with antiplateletes therapy(ASA, plavix)

Not Applicable
Conditions
Epistaxis.
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Registration Number
IRCT201509088872N9
Lead Sponsor
Tehran University of Medical Sciences -Faculty of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

Inclusion Criteria: All patients with epistaxis and history of consumption of ASA and Plavix whom referring to the emergency department.

Exclusion Criteria

Trauma patients; history of anticoagulants drug consumption; Inherited bleeding disorders; Hemophiliacs; Inherited platelet disorders; Shock; Lack of consent; patients with visible bleeding vessel; history of renal disease; INR> 1.5

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding control time. Timepoint: every 5 minutes from the start point until the bleeding stops. Method of measurement: measured by stopwatch, per minute.
Secondary Outcome Measures
NameTimeMethod
Bleeding recurrence. Timepoint: first 24 hours and the first week. Method of measurement: measured by watch.;Patient's satisfaction. Timepoint: within discharge. Method of measurement: by VAS measurment system (10 points mark).
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