American Society of Hirudotherapy
Evidence-Based Medical Resources

American Society of Hirudotherapy

Advancing evidence-based, protocolized use of FDA-cleared medicinal leech therapy and supporting research that closes the regulatory-practice gap in the United States.

3

FDA 510(k) clearances

K040187, K132958, K140907

434+

Salivary proteins identified

Liu et al., 2019

$596M

Bivalirudin peak revenue

Hirudin-inspired FDA-approved drug

78%

Flap salvage rate

Whitaker et al., 2012

What we do

Clinical guidance (scope-limited)

Hospital-centered governance-level guidance for venous congestion workflows, outcomes reporting, and risk framing.

Education

Evidence-informed educational resources for clinicians, including safety protocols, clinical evidence reviews, and leech biology reference materials.

Research agenda (registries / RCT priorities)

Neutral priorities for prospective registries, standard endpoints, and trial concepts where clinical equipoise exists.

Infrastructure project (domestic supply, traceability)

A public-benefit facility concept focused on biosecurity, chain-of-custody documentation, and resilience.

Where nature meets evidence-based medicine

Find What You Need

Resources tailored to your role and interests

FDA-cleared indications are limited; investigational and off-label uses are clearly labeled throughout the site.

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.