Actively Recruiting
Determining the Causes and Outcomes of Febrile Illness in Health Care Facilities in Rural South and Southeast Asia as Part of the SEACTN Network: Work Package B
Led by University of Oxford · Updated on 2026-01-12
7200
Participants Needed
4
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Oxford
Lead Sponsor
S
Shoklo Malaria Research Unit (SMRU)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are studying acute febrile illness in patients older than 28 days who live in rural areas of Laos, Myanmar, Thailand (including the Thai-Myanmar border region), and Bangladesh. This observational study aims to describe the causes, clinical outcomes, and host biomarkers associated with these illnesses, which last 14 days or less. The study is part of a larger community-based network seeking to improve understanding and future interventions for febrile illness in low- and middle-income countries in South and Southeast Asia. The study involves two main parts: Work Package A collects data from village health workers and local health facilities to understand the incidence and outcomes of febrile illness at the community level. Work Package B recruits patients seeking care at higher-level health facilities who may be more severely ill. In Work Package B, researchers collect various samples including venous blood and respiratory specimens for detailed diagnostic testing such as blood cultures, serological assays, molecular diagnostics, and host biomarker assays. Participants will be monitored for about one month to measure the prevalence of pathogens and recovery status. The study will analyze the association between host biomarkers and clinical outcomes to help create electronic decision-support tools for village health workers. These tools and other interventions will be tested later to improve assessment, triage, and treatment of patients with febrile illness. The total duration of participation and follow-up is approximately one month.
CONDITIONS
Brief Title
Causes and Outcomes of Febrile Illness in Health Facilities in Rural South and Southeast Asia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The patient or their guardian is willing and able to give informed consent or assent
- Older than 28 days (day of birth = Day 1)
- Has an axillary temperature of 37.56C (99.56F) or higher, or below 35.56C (95.96F) with no more likely cause than sepsis, or had a fever in the past 24 hours
- Illness started 14 days or less before presentation
You will not qualify if you...
- Illness caused by accident or trauma
- Presentation within 3 days after routine immunisations
- Currently under follow-up or fever-free for less than 72 hours after follow-up
- Healthcare worker decides to send the patient home after initial assessment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 1 month
Participants undergo diagnostic testing including blood cultures, serological assays, pathogen molecular diagnostics, host biomarker assays, and validation of pathogen-blind next generation sequencing approaches to determine the causes of febrile illness.
1 to 2 visits for sample collection
Duration - Approximately 1 month
Participants are monitored for recovery status and clinical outcomes related to febrile illness.
Follow-up visits as needed during the monitoring period
Trial Site Locations
Total: 4 locations
1
Building Resources Across Communities (BRAC)
Dhaka, Bangladesh, 1212
Not Yet Recruiting
2
Laos-Oxford-Mahosot Wellcome Trust Research Unit
Vientiane, Laos, 01000
Actively Recruiting
3
Shoklo Malaria Research Unit
Mae Sot, Changwat Tak, Thailand, 63110
Actively Recruiting
4
Chiangrai Clinical Research Unit (CCRU)
Chiang Rai, Thailand, 57000
Actively Recruiting
Research Team
Y
Yoel Lubell, Prof.
R
Rusheng Chew, Dr.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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