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A research study to reduce the death rate of Russels viper snake bite patients by using Antisnake venom.

Comparing the efficacy and safety of 36 hrs low dose Anti-Snake Venom regimen vs 72 hrs regimen in Russelâ??s viper hemotoxic envenomation - A randomised control trial. - SAVIOR

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/048418
Enrollment
200
Registered
2022-12-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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: POLYVALENT ANTISNAKE VENOM: NOT APPLICABLE Intervention2: POLYVALENT ANTISNAKE VENOM REGIMEN 1: ARM 1 36 HOURS POLYVALENT ANTISNAKE VENOM THERAY FOR RUSSELS VIPER ENVENOMATION. Loading

Sponsors

GOVERNMENT VILLUPURAM MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: (a) Patients aged >18 years with H/o bite by Russelâ??s viper [visually identified] (b) Presenting within 6 hours to our institute. (c) Clinical signs of systemic envenomation warranting ASV, and/or (d) Abnormal WBCT [ >20 minutes, incoagulable].

Exclusion criteria

Exclusion criteria: (a)Patients with CKD (b)Heart failure (c)Pregnancy (d)Age >65 years.

Design outcomes

Primary

MeasureTime frame
MORTALITYTimepoint: 28 DAY

Secondary

MeasureTime frame
1. Dosage of ASV needed 2. Time to normalization of WBCT 3. Time to normalization of PT/INR/APTT. 4. Time to clinical recovery 5. Time to hemodynamic stabilization 6. Need for FFP 7. Dosage of FFP needed 8. Duration of ICU stay. 9. Need for RENAL REPLACEMENT THERAPY 10. Need for Mechanical Vent Support [MVS] 11. Duration of MVS 12. Need for fasciotomy/ amputation. Timepoint: 28 DAY

Countries

India

Contacts

Public ContactSHIVKUMAR GOPALAKRISHNAN

GOVERNMENT VILLUPRAM MEDICAL COLLEGE AND HOSPITAL

gvmcforms123@gmail.com9600778303

Outcome results

None listed

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