CompletedPhase 3NCT00636116
Phase 3 Multicenter Comparative Study to Confirm Safety and Effectiveness of the F(ab)2 Antivenom Anavip.
Studying Snakebite envenomation
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Instituto Bioclon S.A. de C.V.
- Principal Investigator
- Walter García Ubbelohde, MD, MDInstituto Bioclon
- Intervention
- Crotalinae (pit viper) equine immune F(ab)2(biological)
- Enrollment
- 121 target
- Eligibility
- 2-80 years · All sexes
- Timeline
- 2008 – 2012
Study locations (18)
- Banner Good Samaritan Medical Center, Phoenix, Arizona, United States
- Maricopa Integrated Health System, Phoenix, Arizona, United States
- Northwest Medical Center, Phoenix, Arizona, United States
- Tucson Medical Center, Tucson, Arizona, United States
- University Physicians Hospital, Tucson, Arizona, United States
- University Medical Center, Tucson, Arizona, United States
- Loma Linda University Medical Center, Loma Linda, California, United States
- University of California San Diego, San Diego, California, United States
- Rady Children's Hospital, San Diego, California, United States
- Florida Poison Information Center, Jacksonsville, Florida, United States
- Sarasota Memorial Hospital, Sarasota, Florida, United States
- LSU Health Sciences Center, Lousiana Poison Control Center, Shreveport, Louisiana, United States
- The Children's Mercy Hospital, Kansas City, Missouri, United States
- The University of New Mexico Hospital, Albuquerque, New Mexico, United States
- Pitt County Memorial Hospital, Greenville, North Carolina, United States
- +3 more locations on ClinicalTrials.gov
Collaborators
Universidad Nacional Autonoma de Mexico · University of Arizona
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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