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NCT Number: NCT07345910

Environment, Pathogens, and Host Interactions in Melioidosis

This is a longitudinal, multicentre observational study conducted across three established microbiology units integrated within hospital and community health systems in Thailand, Lao PDR, and Cambodia.

The hospital cohort will enroll approximately1,000 patients with positive melioidosis. Participants will be followed at six time points from admission through one year (post-discharge) to capture acute and recovery-phase outcomes, with clinical data collected on demographics, comorbidities, exposures, treatment, adherence, and outcomes.

For each confirmed case, a healthy control will be recruited within two weeks and matched by age, sex, and village of residence. Controls with no symptoms or history of melioidosis will provide a single blood sample at enrolment and will be followed by telephone at 6 and 12 months.

In addition to hospital-based surveillance, a high-risk community in northern Ubon Ratchathani-referred to as the Sandbox Village-will be intensively monitored to capture subclinical infections and to assess environmental factors influencing disease acquisition.

This study is funded by the Wellcome Trust. The grant reference number is 323077/Z/24/Z

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cambodia-Oxford Medical Research Unit (COMRU), Siem Reap, Cambodia

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About this study

This is a longitudinal, multicentre observational study conducted across three established microbiology units integrated within hospital and community health systems:

  • Sunpasitthiprasong Hospital, Ubon Ratchathani, Thailand (MORU);
  • Mahosot Hospital, Vientiane, Lao PDR (LOMWRU); and
  • Angkor Hospital for Children, Siem Reap, Cambodia (COMRU).

In addition to hospital-based surveillance, a high-risk community in northern Ubon Ratchathani-referred to as the Sandbox Village-will be intensively monitored to capture subclinical infections and to assess environmental factors influencing disease acquisition.

Participant Recruitment and Follow-up

Hospital cohort:

Patients with melioidosis will be recruited at all three hospital sites. The study plans to recruit 1,000 patients, who will be followed longitudinally at six time points: Day 0 (admission), Days 3 and 7 (acute phase), and Days 30, 180, and 365 (recovery phase).

Clinical data collected will include demographic characteristics, underlying comorbidities, environmental exposures, lifestyle and behavioural factors, treatment history, patient-reported medication adherence, and follow-up outcomes.

Healthy controls:

Each patient will be matched with a healthy control recruited within two weeks of diagnosis, based on age, sex, and village of residence. Controls will have no current symptoms or prior history of melioidosis. They will provide a single blood sample at enrolment for DNA extraction and antibody profiling and will be followed up by telephone on Days 180 and 365.

Community cohort:

To complement hospital-based data and to identify subclinical infections, intensive community surveillance will be conducted in the Sandbox Village, a high-incidence area within the Ubon Ratchathani region. All residents (approximately 400 individuals) will be enrolled. DNA samples will be collected at baseline, and serum samples will be obtained every two months over a 42-month period, either at participants' homes or at a central village location, to measure antibody responses to Burkholderia pseudomallei as a proxy for exposure.

Community cohort:

To complement hospital-based data and to identify subclinical infections, intensive community surveillance will be conducted in the Sandbox Village, a high-incidence area within the Ubon Ratchathani region. All residents (approximately 400 individuals) will be enrolled. DNA samples will be collected at baseline, and serum samples will be obtained every two months over a 42-month period, either at participants' homes or at a central village location, to measure antibody responses to Burkholderia pseudomallei as a proxy for exposure.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for melioidosis patients:

  • Age ≥20 years
  • Positive for Burkholderia pseudomallei from any clinical samples
  • Resident of the study area for at least two years, including the follow-up period
  • Willing to participate and give informed consent.

Inclusion criteria

for healthy controls:

  • Age ≥20 years
  • Currently healthy as judged by study doctor
  • Resident of the study area for at least two years, including the follow-up period
  • Willing to participate and give informed consent.

Inclusion criteria

for sandbox residents:

  • Age ≥20 years
  • Resident of the study area for at least two years, including the follow-up period
  • Willing to participate and give informed consent.

Exclusion criteria

for melioidosis patients:

  • Current tuberculosis (TB) or TB treatment within the past six months
  • Documented HIV infection or use of immunosuppressive therapy in the past 12 months

Exclusion criteria

for healthy controls:

  • History of melioidosis
  • Significant acute illness
  • Current fever or soft tissue infection

Exclusion criteria

for sandbox residents

-N/A

Treatment and study plan

Primary outcomes

  1. Development of melioidosis following exposure, assessed among melioidosis cases

    Time frame: 365 days

  2. Development of melioidosis following exposure, assessed among healthy controls

    Time frame: 365 days

  3. Development of melioidosis following exposure, assessed among Sandbox Village residents

    Time frame: 3.5 years

  4. Mortality during the acute phase of infection among individuals with melioidosis (melioidosis cases).

    Time frame: 365 days

  5. Number of hospital readmissions following discharge among individuals with melioidosis (melioidosis cases).

    Time frame: 365 days

Secondary outcomes

  1. Changes in disease development following exposure associated with interactions between environmental modifications.

    Time frame: 3.5 years

  2. Changes in mortality during the acute phase of infection following exposure associated with interactions between environmental modifications.

    Time frame: 365 days

  3. Changes in hospital readmission following recovery associated with interactions between environmental modifications.

    Time frame: 365 days

  4. Changes in disease development following exposure associated with interactions between clinical management factors.

    Time frame: 365 days

  5. Changes in mortality during the acute phase of infection following exposure associated with interactions between clinical management factors.

    Time frame: 365 days

  6. Changes in hospital readmission following recovery associated with interactions between clinical management factors.

    Time frame: 365 days

  7. Changes in disease development following exposure associated with interactions involving genetic susceptibility.

    Time frame: 365 days

  8. Changes in mortality during the acute phase of infection following exposure associated with interactions involving genetic susceptibility.

    Time frame: 365 days

  9. Changes in hospital readmission following recovery associated with interactions involving genetic susceptibility.

    Time frame: 365 days

Study contacts

Contact information is provided by the study sponsor or research team.

Kamolchanok Claire Chewapreecha, PhD

CONTACT

[email protected]

662 203 6333

Sponsors and collaborators

Lead sponsor

University of Oxford

Other

Registry information

Official study title

Decoding the Triad: the Interplay Between Environment, Pathogen, and Host in Melioidosis (DeEPH)

Acronym: DeEPH

Important dates

Study start
2026
Primary completion
2034
Study completion
2034
First posted
Jan 16, 2026
Registry last updated
Jan 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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