Amerikanische Gesellschaft für Hirudotherapie

Hirudo (Leech) for proliferative vitreous retinopathy: A protocol for systemic review and meta-analysis

Huang H, Lei R, Li Y, Huang Q, Gao N, Zou W (2021) · Medicine (Baltimore) · n=0

RCT-EvidenzdetailsStudienreferenz
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Studienprofil

Design
pre-registered systematic review and meta-analysis protocol for Hirudo (leech) or Hirudo-containing Chinese compound prescriptions in proliferative vitreous retinopathy (Chengdu University of Traditional Chinese Medicine, China)
Stichprobengröße (n)
Intervention
Planned synthesis of randomized controlled trials in English or Chinese on Hirudo (leech) and Hirudo-containing compound prescriptions for proliferative vitreous retinopathy (PVR)
Komparator
Cross-trial: conventional ophthalmologic care without Hirudo product
Primärer Endpunkt
Change in vitreous opacity, vision changes, anterior macular membrane formation, retinal detachment recurrence, and adverse-event incidence
Primäres Ergebnis
Pre-registered protocol only - no results yet available; protocol registered at OSF (10.17605/OSF.IO/FP7VG); planned 8-database search including Cochrane, PubMed, MEDLINE, EMBASE, CNKI, CBM, VIP, and Wanfang
Follow-up-Dauer
to be determined per included studies

Wichtigste Ergebnisse

  • First pre-registered systematic review protocol for Hirudo/leech-containing therapeutics in proliferative vitreous retinopathy
  • Plans to incorporate Chinese-language databases (CNKI, CBM, VIP, Wanfang) often missing from Western reviews
  • Includes both whole-leech therapy and Hirudo-containing Chinese herbal compound prescriptions in scope
  • Documents the emerging investigation of leech-derived therapeutics in ophthalmologic indications outside the FDA K040187 clearance
  • Pre-registration at OSF supports methodological transparency

Einschränkungen

  • Protocol only - no results available at time of registry inclusion
  • Scope conflates whole-leech therapy with multi-ingredient Chinese herbal compound prescriptions - mechanistic specificity reduced
  • Chinese-language source heterogeneity may produce quality challenges
  • PVR is a niche ophthalmologic indication - generalizability to broader leech-therapy literature limited
  • Investigators are from a single Chinese TCM institution - external validation pending

Klinische Implikationen

Huang 2021 is a pre-registered systematic review protocol on Hirudo (leech) therapeutics for proliferative vitreous retinopathy. The trial is included in this registry to document the emerging Chinese investigation of leech-derived ophthalmologic indications - a use case largely absent from the Western FDA-cleared K040187 framework. The protocol's ultimate publication will be informative for understanding the global leech-therapy evidence base. ASH editorial team should track the eventual full-publication output of this systematic review.

Verwandte Studien

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