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Ivermectin is better than benzyl benzoate for childhood scabies in developing countries
1Outpatients Department, Vila Central Hospital, Port Vila, Vanuatu. pdbrooks@netscape.net.au
Insights
Single dose oral ivermectin and topical benzyl benzoate showed similar effectiveness for treating pediatric scabies. Ivermectin is a preferred treatment for scabies in developing nations due to its safety and additional antiparasitic benefits.
Area of Science:
- Dermatology
- Parasitology
- Tropical Medicine
Background:
- Scabies is a contagious skin infestation caused by the mite Sarcoptes scabiei.
- Pediatric scabies presents a significant public health challenge, particularly in developing countries.
- Topical benzyl benzoate and oral ivermectin are common treatment options.
Purpose of the Study:
- To compare the efficacy and safety of single-dose oral ivermectin versus topical benzyl benzoate for treating pediatric scabies.
- To evaluate treatment outcomes based on lesion count, itch scores, and adverse events.
Main Methods:
- An observer-blinded randomized controlled trial was conducted with 110 children (6 months to 14 years).
- Participants received either oral ivermectin (200 micro g/kg) or 10% topical benzyl benzoate.
- Outcomes were assessed at 3 weeks post-treatment, including lesion count, itch, and side effects.
Main Results:
- Both ivermectin and benzyl benzoate significantly reduced scabies lesions and itch.
- Ivermectin achieved a cure rate of 56% (24/43), while benzyl benzoate achieved 51% (19/37).
- Benzyl benzoate was associated with a higher incidence of local skin reactions (P = 0.004).
Conclusions:
- Oral ivermectin is a safe and effective treatment for pediatric scabies.
- Ivermectin offers additional antiparasitic benefits and is recommended over benzyl benzoate in developing countries.
- Both treatments demonstrated significant efficacy, but ivermectin showed a better safety profile regarding skin reactions.
Objective:
To compare single dose oral ivermectin with topical benzyl benzoate for the treatment of paediatric scabies.
Methods:
An observer-blinded randomized controlled trial was undertaken at Vila Central Hospital, Vanuatu. One hundred and ten children aged from 6 months to 14 years were randomized to receive either ivermectin 200 micro g/kg orally or 10% benzyl benzoate topically. Follow up was at 3 weeks post-treatment. Primary outcome measures were the number of scabies lesions, the itch visual analogue score and nocturnal itch. Secondary outcome measures were the skin's reaction to treatment, the passage of worms in stool and other side effects.
Results:
Eighty patients completed the study protocol. There was no significant difference between the two treatments; both produced a significant decrease in the number of scabies lesions seen at follow up. Ivermectin cured 24 out of 43 patients (56%), and benzyl benzoate 19 out of 37 patients (51%) at 3 weeks post-treatment. No serious side effects were noted with either treatment, but benzyl benzoate was more likely to produce local skin reactions (P = 0.004, OR 6.4, 95% CI 1.6-25.0)
Conclusions:
Ivermectin is cheap and effective in the treatment of paediatric scabies. Ivermectin has minimal observed toxicity and has the additional beneficial effects of antiparasitic action in onchocerciasis, filariasis and strongyloidiasis. Ivermectin is better than benzyl benzoate for the treatment of paediatric scabies in developing countries.
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