American Society of Hirudotherapy

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Faceted search across all 5 registries. Filter by registry type, evidence level, or safety domain.

Curated knowledge libraryReference collection

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This library indexes the full evidence base. For orientation, begin with the core guides:

Conditions

10

Venous Congestion in Surgical Flaps

Tier A

FDA-cleared application: medicinal leech therapy to relieve venous congestion in compromised tissue flaps awaiting vascular ingrowth.

FDA-cleared device indicationFDA-cleared regulatory context

Microsurgical Replantation (Digit / Ear / Scalp)

Tier A

FDA-cleared application: post-replantation venous decompression in digits, ears, scalp, and partial avulsion injuries.

FDA-cleared device indicationFDA-cleared regulatory context

Breast Reconstruction Flap Salvage

Tier A

FDA-cleared application: venous decompression of compromised DIEP, TRAM, and latissimus dorsi flaps in post-mastectomy reconstruction.

FDA-cleared device indicationFDA-cleared regulatory context

Chronic Venous Insufficiency (CEAP C3-C5)

Tier B

Off-label adjunct to compression; the evidence is one small open-label randomized trial in varicose veins (n=50) and a 20-patient uncontrolled series.

Studied off-labelRCT

Venous Leg Ulcer

Tier B

Off-label adjunct to compression therapy; the evidence is one 20-patient uncontrolled series in complicated varicose veins plus case reports.

Studied off-labelCohort / case series

Post-Thrombotic Syndrome

Tier C

Investigational use; no controlled trial was identified, and the only clinical report is a 1998 conference series of 87 patients without a comparison group.

InvestigationalInsufficient evidence

Lumbar Radiculopathy (Sciatica)

Tier C

Investigational use for lumbar radiculopathy; the closest randomized evidence is in chronic low back pain (Hohmann 2018, n=44), not radicular pain.

InvestigationalRCT

Congestive Heart Failure (Compensated, Investigational Adjunct)

Tier C

Investigational adjunct in compensated NYHA II heart failure; only small open-label or uncontrolled studies were identified, mostly in Russian-language sources; guideline-directed medical therapy remains primary.

InvestigationalCohort / case series

Adenomyosis (Investigational Palliative Adjunct)

Tier C

Investigational palliative adjunct for adenomyosis-related dysmenorrhea and pelvic pain; hormonal therapy (LNG-IUD, dienogest, GnRH antagonists) and (definitively) hysterectomy remain evidence-based.

InvestigationalCohort / case series

Myalgic Encephalomyelitis / Chronic Fatigue Syndrome (Investigational Adjunct)

Tier C

Investigational adjunct for ME/CFS symptom management; pacing strategies, post-exertional malaise avoidance, and individualized supportive care remain primary; graded exercise therapy is no longer recommended per updated NICE guidance.

InvestigationalInsufficient evidence

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.

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