Skip to content

Effects of antivenom for local limb swelling reduction in patients envenomated by green pit viper: double-blinded randomised controlled trial

Effects of antivenom for local limb swelling reduction in patients envenomated by green pit viper: double-blinded randomised controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20211027005
Enrollment
40
Registered
2021-10-27
Start date
2021-09-23
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Bitten by green pit viper Limb swelling at least to nearest joint No systemic indications for antivenom Snake Bite Snake Envenoming Antivenins Extremities Edema

Interventions

Patients enrolled in this arm were received 3 vials of monovalent green pit viper antivenom dissolved in 50 mL of NSS which are slowly dripped IV in 30 minutes.,Patients enrolled in this arm were rece
Active Comparator Drug,Placebo Comparator Drug
Antivenom,Placebo

Sponsors

Siriraj Routine to Research Unit
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Bitten by green pit viper diagnosed by fang mark plus at least one of the followings : bring the bitten snake or describe the characteristics of the snake correctly - Bitten at upper or lower limb and swelling of bitten area up to nearest joint (if bitten at hand, foot, finger, or toe then the swelling area must reach wrist or ankle)

Exclusion criteria

Exclusion criteria: - Having other clear indications for antivenins - Patients taken any antiplatelet or anticoagulant medication - Patients have underlying disease associated with abnormal hemostasis - Patients cannot clearly identified bitten snake as indicated in inclusion criteria

Design outcomes

Primary

MeasureTime frame
Local limb swelling reduction 6 hours after intervention % limb swelling reduction

Secondary

MeasureTime frame
Pain reduction 6 hours after intervention Pain score,Hospital length of stay After discharge Days of hospital,Incidence of hypersensitivity reaction 14 days after intervention Observation,Incidence of wound infection 14 days after intervention Observation

Countries

Thailand

Contacts

Public ContactKorakot Suvanges

Department of Surgery, Faculty of Medicine Siriraj Hospital, Mahidol University

kor.svg@gmail.com0909876280

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026