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Anti nosebleeds effect of Achillia ointment

Phase 3
Conditions
Epistaxis.
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Registration Number
IRCT201410303186N6
Lead Sponsor
Vice Chancellor for Research and Technology of Hamadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Inclusion critria: the patients who referred to the clinic of Besat hospital with recurrent epistaxis (minimum of 3 times per 2 months) and no specific etiology detect on history and physical exam
Exclusion criteria:
1- Age under 12 and above 50 years old.
2- Pregnancy.
3- OCP use.
4- Hx of ischemic heart disease.
5- Hx of hypertension.
6- Hx of thromboamboli.
7- Hx of allergy to Achillia
8- Coagulation disorder.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: Day 11th, fisrt month and third month after drug administration. Method of measurement: Epistaxis Severity score.
Secondary Outcome Measures
NameTimeMethod
Adverse effect. Timepoint: Day 11th, first month and third month after drug administration. Method of measurement: History and clinical examination.
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