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Effect dressing material on blood clotting time.

Not Applicable
Registration Number
CTRI/2021/04/033048
Lead Sponsor
alit Kumar
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Blood will be collected from volunteers of 18 to 60 age group population (each age group contains 10 subjects).

c) Statistical methods: T-test and one-way ANOVA will be used to compare the results between different age groups in the presence of hemostatic composition.

Exclusion Criteria

A detailed history will be collected, and the subjects with any hemostatic or thrombotic challenges like pregnancy/postpartum or liver disease will be excluded from the study. Subjects who are on medication which were known to influence the hemostatic mechanism (nonsteroidal anti-inflammatory drugs, antihistamines, antiplatelet drugs) will be excluded.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood clotting time in presence of hemostatic polymersTimepoint: Blood clotting time in presence of hemostatic polymers after 8 weeks
Secondary Outcome Measures
NameTimeMethod
Among different compositions best composition can be reportedTimepoint: Clotting time after 8 weeks
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