Actively Recruiting

Age: 29Days +
All Genders
ID04629053

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

Age: 29Days +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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