Development, Validation and Clinical Efficacy Evaluation of an AI-based Snake Species Identification System for Snakebite Treatment: a Multicenter Prospective Observational Study
Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University
Trial Details
| Condition | Snake Bite |
| Intervention | SSRS system-assisted snake species identification |
| Status | Unknown |
| Participants | 400 |
| Est. Completion | 20 June 2026 |
| Last Updated | 22 June 2026 |
Primary Outcome
Snake species identification (64-class classification) and venomous/non-venomous snake discrimination (binary classification)
Eligibility Criteria
Inclusion Criteria
Inclusion Criteria: 1. Adult patients aged ≥18 years, regardless of gender 2. Definite history of snake bite, with time from bite occurrence to first medical visit ≤24 hours 3. The patient or eyewitness can provide digital images of the biting snake (taken by mobile phone, camera, etc.) 4. Voluntarily sign the written informed consent form; for patients with impaired consciousness who cannot sign independently, their legal representative shall sign on their behalf, and a secondary confirmation shall be obtained after the patient regains consciousness 5. Able to cooperate in completing follow-up assessments at discharge and 30 days after injury Exclusion Criteria: * 1\. Unable to provide snake images, or images are severely blurred resulting in complete loss of key identification features 2. Snake species cannot be confirmed by the gold standard (no eyewitnesses, no typical clinical manifestations, cannot be clarified by expert panel consultation) 3. Medical visit exceeds 24 hours and the exact bite time and initial clinical manifestations cannot be determined 4. Complicated with end-stage malignant tumors, severe liver and kidney failure, or other underlying diseases that may significantly affect prognosis judgment 5. Refuse to sign the informed consent form or cannot cooperate in completing follow-up 6. Simultaneously participating in other clinical studies that may affect the results of this study
Trial Sites
Countries
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