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NCT ID: NCT03236168 Completed - Scabies Clinical Trials

Impact of Community Scabies Treatment on Head Lice Prevalence in the Solomon Islands

Start date: August 1, 2017
Phase: Phase 3
Study type: Interventional

This is a pilot study evaluating if treatment for scabies also treats headlice in the same community

NCT ID: NCT02775617 Completed - Scabies Clinical Trials

Azithromycin - Ivermectin Mass Drug Administration for Skin Disease

AIM-Skin
Start date: July 2016
Phase: Phase 4
Study type: Interventional

This is an open-label prospective community intervention trial to assess the impact of community mass treatment with azithromycin for yaws and ivermectin for scabies, on non-yaws bacterial skin infections. Communities will be randomised to receive standard treatment for both yaws and scabies either in parallel (site 1) or in sequence (site 2). Treatment of yaws: Single dose of Azithromycin (30mg/kg, max 2G). Treatment of scabies: Either an oral dose of Ivermectin (200μg/kg) or permethrin cream for those with a contraindication to Ivermectin (WT<15kg, pregnant or breastfeeding women) given in 2 doses 7-14 days apart. Investigators will complete a clinical and microbiological assessment of bacterial skin disease at baseline and at 12 months to assess the impact of treatment on the prevalence of bacterial infection and the emergence of antimicrobial resistance. Primary Outcome 1. Difference in the change in prevalence of impetigo between baseline and 12- months between the parallel and the sequential treatment arms. Secondary Outcomes 2. Change in the proportion of swab samples from which S. pyogenes is cultured between baseline and follow-up in the two arms 3. The proportion of samples from which a drug-resistant isolate of S.pyogenes is cultured in the two arms