Clinical Trials Directory

Trials / Recruiting

RecruitingNCT04478578

Incidences, Causes, and Outcomes of Febrile Illness in Rural South and Southeast Asia

Determining the Incidence, Causes and Outcomes of Rural Febrile Illness (RFI) in South and Southeast Asia, as Part of the South and Southeast Asian Community-based Trials Network (SEACTN). Work Package A (WP-A).

Status
Recruiting
Phase
Study type
Observational
Enrollment
100,000 (estimated)
Sponsor
University of Oxford · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The study will collect information to understand the causes and outcomes of febrile illness in rural areas in countries across South and Southeast Asia ( including Cambodia, Laos, Myanmar and Bangladesh). The findings will be used to identify new tests and treatments that can improve the management of febrile patients in the future. This study is funded by the UK Wellcome Trust. The grant reference number is 215604/Z/19/Z

Detailed description

This study aims to better understand and quantify the burden of febrile illness, the aetiological causes and the manner in which it affects the people living in rural areas in South and Southeast Asia, all on a scale which has not been attempted before. The SEACTN RFI project will collect information to help better understand and predict these outcomes based on a multitude of factors, which will form the basis for interventions within the network in the future. Determining the incidence, causes and outcomes of febrile illness in these settings will be done through two work packages. The first of these, Work Package A (WP-A), the subject of this study, will be carried out at the community level, primarily by engaging village health worker (VHWs) and low-level Health Centres (HCs) which serve the communities to recruit patients presenting with a febrile illness. These patients will be assessed for presenting symptoms and followed up for clinical outcomes. Collection of specimen for diagnostic investigations in these settings is challenging. Currently, mRDTs are conducted by VHWs and HCs in these networks, therefore by using the same process, but also applying blood to filter paper and allowing it to dry (DBS), investigators will test for certain other pathogens, which will increase the aetiological yield.

Conditions

Timeline

Start date
2021-08-04
Primary completion
2024-12-01
Completion
2024-12-30
First posted
2020-07-20
Last updated
2024-05-09

Locations

7 sites across 5 countries: Bangladesh, Burma, Cambodia, Laos, Thailand

Source: ClinicalTrials.gov record NCT04478578. Inclusion in this directory is not an endorsement.