Maggot Therapy for Wound Debridement: A Randomized Multicenter Trial | Hypertension | JAMA Dermatology | JAMA Network
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Apr 2012

Maggot Therapy for Wound Debridement: A Randomized Multicenter Trial

Author Affiliations

Author Affiliations: Department of Dermatology (Drs Opletalová, Laplaud, Sohyer-Lebreuilly, and Dompmartin and Ms Mourgeon), and Biostatistics and Clinical Research Unit, Clinical and Epidemiological Research Department (Drs Blaizot and Creveuil and Mr Chêne), Université de Caen Basse-Normandie, Centre Hospitalier Universitaire de Caen, Caen, France; and Department of Dermatology, Hôpital Desgenettes, and Regional Center Léon Bérard, Lyon, France (Dr Combemale).

Arch Dermatol. 2012;148(4):432-438. doi:10.1001/archdermatol.2011.1895

Objective To study the efficacy of bagged larvae on wound debridement compared with conventional treatment.

Design Randomized, multicenter, controlled, prospective phase 3 trial with blinded assessment of outcome measures by a single observer.

Setting Two hospital referral centers in Caen and Lyon, France.

Patients Random sampling of 119 patients with a nonhealing, sloughy wound 40 cm2 or smaller, less than 2 cm deep, and an ankle brachial index of 0.8 or higher.

Intervention During a 2-week hospital stay, patients received either maggot debridement therapy (MDT) or conventional treatment. At discharge, conventional dressings were applied and a follow-up visit occurred at day 30.

Main Outcome Measure Percentage of slough in wounds at day 15.

Results There was a significant difference between groups at day 8 (54.5% in the MDT group and 66.5% in the control group) (P = .04). The mean percentage of slough at day 15 was 55.4% in the MDT group and 53.8% in the control group (P = .78).

Conclusions Although MDT shows no significant benefit at day 15 compared with conventional treatment, debridement by MDT is significantly faster and occurs during the first week of treatment. Because there is no benefit in continuing the treatment after 1 week, another type of dressing should be used after 2 or 3 applications of MDT.

Trial Registration Identifier: NCT01211236