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Analysis of coagulability and coagulation factors before and after the development of symptoms in patients with physical urticaria

Not Applicable
Conditions
physical urticaria
Registration Number
JPRN-UMIN000002585
Lead Sponsor
Department of Dermatology, Hiroshima University Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

1. Pregnant or lactating women or women of child bearing potential not using contraception 2. Patients with diseases as follows. Liver disease, psychological illness, convulsive and other seizure, heart disease, hemoglobinopathy, hemophilia, uncontrolled diabetes, and autoimmune diseases. 3. Patients who use medications that influence the coagulation and fibrinolytic cascade. 4. Others whom the physician judges are not suitable as subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measurements regarding coagulability, coagulation factors and levels of blood histamine before and after the development of symptoms
Secondary Outcome Measures
NameTimeMethod
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