About this trial

The goal of this Phase III clinical trial is to evaluate the efficacy, safety, and acceptability of different treatment regimens for Trichuris trichiura infection in schoolchildren aged 6 to 15 years living in La Moskitia, Honduras, an area with a high burden of soil-transmitted helminth infections.

The main questions it aims to answer are:

* Are combination treatments of albendazole and ivermectin more effective than albendazole alone for treating Trichuris trichiura infection? * Does a fixed-dose combination (FDC) of albendazole and ivermectin achieve cure rates comparable to co-administration of the two drugs? * How effective are the different treatment regimens against other soil-transmitted helminths, including Strongyloides stercoralis? * What adverse events occur following treatment with the different regimens? * How acceptable are the different treatment regimens to children and their caregivers?

Researchers will compare four treatment groups: placebo, albendazole alone, albendazole plus ivermectin, and a fixed-dose combination of albendazole plus ivermectin.

Participants will:

* Be randomly assigned to one of the four treatment groups. * Receive a single dose of the assigned treatment. * Provide stool samples before treatment and approximately 21 days after treatment. * Undergo laboratory testing using quantitative real-time PCR (qPCR) to detect and quantify helminth infections. * Be monitored for adverse events after treatment. * Complete acceptability assessments together with their caregivers.

The study will provide evidence on the efficacy, safety, and acceptability of a fixed-dose combination of albendazole and ivermectin and its potential use as a simplified treatment strategy for the control of soil-transmitted helminth infections in endemic settings.

Eligibility criteria

Qualifiers

Trichuris trichiura infection documented by quantitative real-time PCR (qPCR) performed within 30 days prior to randomization.

Age 6 to 15 years inclusive.

Written informed consent provided by a parent or legal guardian. Assent provided by children aged 9 years or older, according to local ethical requirements.

Disqualifiers

Known allergy or hypersensitivity to albendazole or ivermectin.

Receipt of an anthelmintic treatment (albendazole, mebendazole, or ivermectin) within 3 months prior to enrollment.

Participation in another clinical trial within 3 months prior to enrollment.

Severe comorbidity at the investigator's discretion (e.g., diarrhea, tuberculosis, or malaria).

Trial design

Treatments tested in this trial

  • Placebo
  • Albendazole 400 mg
  • Albendazole Plus Ivermectin
  • Fixed-Dose Combination Albendazole/Ivermectin (FDC)

Treatment groups

368 Participants
are divided into 4 treatment groups

Locations

1
Instituto de Investigaciones en Microbiología, Facultad De Ciencias, Universidad Nacional Autónoma de Honduras11101, Tegucigalpa Honduras

Sponsors and collaborators

Mundo Sano Foundation

Lead sponsor