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Adjustment of antisnake venom dose in snake bite poisoning

Development and Optimization of Anti snake venom dosing strategies in snakebite envenomated patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/067306
Enrollment
400
Registered
2024-05-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: T630- Toxic effect of snake venom

Interventions

Intervention1: NIL: NIL

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients (aged =18 years) irrespective of gender and admitted to the hospital with snake bite envenomation and on therapy with ASV.

Exclusion criteria

Exclusion criteria: 1.Patients who were managed with supportive therapy alone 2. Patients referred from other centres with the history of snakebites with concomitant hospital acquired infections. 3.Patients with history of snakebite more than 10 days and referred for further management.

Design outcomes

Primary

MeasureTime frame
Primary outcome is the effectiveness of ASV treatment dosing in terms of recovery/mortality Timepoint: Assessment done at 2 time points: Time of enrollment and at the time of discharge

Secondary

MeasureTime frame
Evaluation of -ventilation -oxygenation -hospitalization days -severity scores -laboratory parameters -weaning of vasopressors Safety would be assessed by monitoring for any adverse reactions due to ASV in patientTimepoint: Assessment done at 2 time points: Time of enrollment and at the time of discharge

Countries

India

Contacts

Public ContactGirish Thunga

Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka

girish.thunga@manipal.edu9880151127

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026