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Fresh Frozen Plasma treatment in Russell's viper bite

Not Applicable
Recruiting
Conditions
Snake bite
Registration Number
SLCTR/2010/011
Lead Sponsor
South Asia Clinical Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

a) Suspected or confirmed Russell’s viper bite
b) Venom induced consumption coagulopathy defined as: WBCT > 20 minutes
c) No known hypersenstivity to blood products
d) FFP is available and can be given to the patient within 4 hours of commencing antivenom

Exclusion Criteria

a) Age < 16 years
b) Pregnancy
c) Definite bite by a snake other than a Russell’s viper

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome will be the proportion of patients with a return of near-normal coagulation function defined by an INR < 2.0 measured (6 hours after antivenom treatment was commenced)<br> [6 hours after antivenom treatment]<br>
Secondary Outcome Measures
NameTimeMethod
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