Sociedad Americana de Hirudoterapia

Clinical Efficacy of Leech Therapy (Ta'liq al-'Alaq) in Eczema (Nar Farsi): An Open-Label Single-Arm Clinical Study

Ulla P BS, Aaisha B, Bokhari S, Zabiulla P, Alam MA, Nikhat S (2025) · Alternative Therapies in Health and Medicine · n=20

RCT evidence detailTrial reference
GRADE Very LowInsufficient evidenceCondition: Knee Osteoarthritis
Sample size of this trial compared with other Knee Osteoarthritis trialsWang H 2018264Lauche R 2025240Lauche R 2014237Farzali S 2025181Cui Y 2024144Andereya S 2008113Andereya S 2008113Sarbaev IS 201996Isik M 201790Ulla P BS 202520
This trial (highlighted) by sample size alongside other indexed Knee Osteoarthritis trials. Larger trials generally carry more statistical weight.

Study Profile

Design
single-center, open-label, single-arm clinical study of leech therapy for eczema in the Unani medicine tradition (India)
Sample size (n)
20
Intervention
Four sessions of leech therapy with one-week intervals; standardized Ta'liq al-'Alaq (leech therapy) protocol per Unani medicine practice
Comparator
Within-subject pre/post comparison using standardized Eczema Area and Severity Index (EASI) - no randomized control arm
Primary endpoint
Eczema Area and Severity Index (EASI) score - components for redness, edema, excoriation, lichenification, and total area
Primary result
Statistically significant improvement in eczema severity: redness (p=0.0001), edema (p=0.0001), excoriation (p=0.0022), lichenification (p=0.0001); total area involved did not show statistically significant decrease (p=0.24); all 20 patients completed the trial with no dropouts
Follow-up duration
4 weekly sessions (~28 days)

Key Findings

  • First PubMed-indexed Unani medicine clinical trial of leech therapy for eczema (Nar Farsi)
  • Significant within-subject improvements in three of four EASI components (redness, edema, excoriation, lichenification)
  • Total skin area involvement did not significantly decrease - suggests symptomatic improvement without disease-modifying area reduction
  • 100% completion rate (no dropouts) signals patient acceptability of multi-session leech protocol
  • Provides hypothesis-generating signal for leech therapy in inflammatory dermatologic conditions

Limitations

  • Single-arm design with no randomized control - entire effect could reflect natural fluctuation, placebo, or attention
  • Small sample (n=20)
  • Open-label evaluation by treating clinicians who knew the intervention
  • Single Unani medicine institution - selection bias toward CAM-favorable patient population
  • Eczema is a relapsing-remitting condition - 4-week follow-up cannot assess durability

Clinical Implications

Ulla 2025 is the only PubMed-indexed Unani-medicine clinical study of leech therapy for eczema and provides exploratory evidence that leech application may improve inflammatory eczema parameters. The single-arm uncontrolled design limits causal inference, and the lack of total-area improvement suggests symptomatic-only effect. For ASH editorial purposes, this study is cited only as preliminary cross-cultural evidence; it does not support routine use in eczema. The trial illustrates the broader Unani medicine application of leech therapy across dermatologic indications - a use case largely absent from the Western evidence base.

Related Trials

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.