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Does a lower dose of antisnake venom work as well as the standard dose in patients with krait snakebite

Low-dose versus standard-dose antisnake venom in common krait envenomation : A randomized non inferiority trial - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108508
Enrollment
76
Registered
2026-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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: Low Dose Anti Snake Venom: Patients with Common Krait envenomation who are enrolled in Intervention arm will receive initial dose of 6 vials of Indian Polyvalent Antisnake Venom over 30

Sponsors

Postgraduate Institute of Medical Education and Research PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age more than 12 years 2.Clinical diagnosis of common krait envenomation 3.Neuroparalytic manifestations attributable to snake envenomation. 4.Snakebite to initiation of ASV therapy less than or equal to 12 hours

Exclusion criteria

Exclusion criteria: 1.Evidence of hemotoxic envenomation (abnormal 20-minute WBCT or laboratory-confirmed coagulopathy) 2.Prominent local swelling or necrosis suggestive of cobra envenomation 3.Dry or incomplete bite without neurotoxicity 4.Completed ASV treatment in an outside hospital 5.Refusal of consent

Design outcomes

Primary

MeasureTime frame
Ventilator free days at day 7 (VFD7)Timepoint: Day 7 after enrolment

Secondary

MeasureTime frame
Time to recovery from neurotoxic paralysis defined as sustained resolution of bulbar ocular limb & respiratory muscle weaknessTimepoint: Up to discharge from hospital;Total hospital length of stay in daysTimepoint: At hospital discharge;In hospital mortalityTimepoint: During hospital stay;Antivenom related adverse reactions including acute hypersensitivity reactions & delayed reactionsTimepoint: During hospital stay

Countries

India

Contacts

Public ContactDr Ashok Kumar Pannu

Post Graduate Institute of Medical Education and Research, Chandigarh

gawaribacchi@gmail.com9914291115

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026