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Blood Tests Measuring Tuberculosis DNA to Track Treatment Response

Studies whether tuberculosis DNA in the blood can show how treatment is working.

Plain-language title generated from the registry record
Registry title: Blood Tuberculosis DNA Levels to Monitor Tuberculosis Treatment

Key facts

Where
Tak, ThailandSee the site

Where in Thailand

  • Shoklo Malaria Research Unit (SMRU)Tak, ThailandTaking people

Questions to ask the study team

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  2. Are travel costs paid?
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  4. What happens if I want to stop?
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Trial details

Who runs it
University of Oxford
Trial code
NCT06845618
Record updated
13 April 2026
Original description
Tuberculosis (TB) is a leading infectious cause of death worldwide. Current strategies for monitoring TB treatment response are culture dependent and insensitive. New methods of assessing treatment response in vivo could inform new drug development and other treatment strategies. Cell-free DNA (cfDNA) - small circulating fragments of DNA - is widely used in maternofetal medicine and oncology for diagnosis and assessment of treatment response. This study aims to investigate whether pathogen derived Mycobacterium tuberculosis-specific cfDNA (Mtb-cfDNA) can be used to monitor TB treatment response.Read full original descriptionShow less

Mycobacterium Tuberculosis Complex Cell-free DNA (Mtb-cfDNA) for the Pharmacometric Assessment of Anti-tuberculosis Treatment: a Proof-of-concept Study

Tuberculosis (TB) is a leading infectious cause of death worldwide. Current strategies for monitoring TB treatment response are culture dependent and insensitive. New methods of assessing treatment response in vivo could inform new drug development and other treatment strategies. Cell-free DNA (cfDNA) - small circulating fragments of DNA - is widely used in maternofetal medicine and oncology for diagnosis and assessment of treatment response. This study aims to investigate whether pathogen derived Mycobacterium tuberculosis-specific cfDNA (Mtb-cfDNA) can be used to monitor TB treatment response.

This feasibility study will take place at Mae RaMat TB Center in Thailand and includes two study groups:

1. Assay Development and Validation 2. Longitudinal Assessment of Mtb-cfDNA levels

Inclusion: Participants with a new diagnosis of tuberculosis; Aged ≥ 18 years old; Newly microbiologically confirmed (culture or nucleic acid amplification test) diagnosis of Mycobacterium tuberculosis (Mtb.) infection (of any site); Has not yet commenced antituberculosis therapy; Able to understand study procedures and requirements and is able to give informed consent; For healthy volunteers:; Aged ≥ 18 years old; Healthy as judged by a responsible physician; Able to understand study procedures and requirements and is able to give informed consent.

Exclusion: Participants with a new diagnosis of tuberculosis; Exposure to antituberculosis treatment in the last 8 weeks (or Mycobacterium tuberculosis (Mtb.) active fluoroquinolone); Known history of underlying malignancy; History of tuberculosis infection or latent tuberculosis infection; Household, or other close contact, of a person living with tuberculosis disease; Chest radiograph (CXR) changes suggestive of pulmonary tuberculosis; Presence of symptoms which would otherwise indicate screening for tuberculosis (cough > 2 weeks duration, fever, weight loss, night sweats); Known malignancy; Pregnancy; Transfusion dependent anaemia; For healthy volunteers:; Other major medical comorbidity; Pregnancy.

ClinicalTrials.gov NCT06845618