None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
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
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood clotting time in presence of hemostatic polymersTimepoint: Blood clotting time in presence of hemostatic polymers after 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Among different compositions best composition can be reportedTimepoint: Clotting time after 8 weeks | — |
Countries
India
Contacts
Manipal college of pharmaceutical sciences