跳至主要内容
临床试验/CTRI/2026/03/105674
CTRI/2026/03/105674Not Applicable4 期

Effectiveness of Different Scabies Control Interventions among Madrasa Students of Tungipara Sub-district, Bangladesh

Dr Tanvir Ahmed1 个研究点 分布在 1 个国家目标入组 1,600 人开始时间: 2026年3月17日最近更新:

试验速览

阶段
4 期
状态
Not Applicable
发起方
入组人数
1,600
试验地点
1

研究概览

简要总结

Scabies is a parasitic skin infestation caused by Sarcoptes scabiei affecting millions worldwide particularly in overcrowded settings like madrassas in Bangladesh. This cluster randomized controlled trial aims to compare the effectiveness of different public health approaches for controlling scabies among madrassa students in Tungipara Subdistrict Bangladesh.

A total of 16 madrassas with approximately 1600 participants will be randomly allocated to four intervention groups. Arm A receives Mass Drug Administration plus health education with either Permethrin 5 percent cream or Oral Ivermectin (200 microgram per kg body weight). Arm B receives targeted therapy (cases and close contacts only) plus health education with the same drugs. Topical Permethrin is applied overnight for two rounds seven days apart. Oral Ivermectin is taken on empty stomach for two rounds seven days apart.

The primary outcome is point prevalence of active scabies at one month post intervention. Secondary outcomes include prevalence and reinfestation rates at 06 and 12 months adverse events acceptability adherence changes in hygiene related knowledge attitudes and practices cost effectiveness and barriers and facilitators to program implementation.

This study will provide evidence on optimal public health strategies for scabies control in high risk institutional settings and inform routine program implementation in Bangladesh.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
5.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • All students teachers and staff of participating madrassas who are aged 5 years or above and residing in the boarding facility.

排除标准

  • Known allergies or contraindication to permethrin or oral ivermectin; Received treatment for scabies within last 14 days; Pregnancy (for ivermectin groups); Body weight below 15 kg (for ivermectin groups) ; Non-boarding madrassa students; Madrassas currently in any scabies or other skin treatment program; Madrassas not willing to participate.

研究者

发起方
Dr Tanvir Ahmed
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Tanvir Ahmed

Office of the Upazila Health and Family Planning Officer

研究点 (1)

Loading locations...

相似试验