Evaluation of PATHFAST-LAM as a Tuberculosis Treatment Monitoring Tool in Kenya
NCT ID: NCT07157904
Last Updated: 2025-09-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
300 participants
OBSERVATIONAL
2026-01-31
2027-07-31
Brief Summary
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The primary objective of this study is to assess whether changes in sputum LAM levels can help predict unfavorable results.
In this study, investigators will recruit adult patients diagnosed with pulmonary TB from multiple healthcare facilities in Nairobi, Kenya. Investigators will follow them during their TB treatment and collect sputum and urine samples at the beginning of treatment, then, every week for the first month, every two weeks for the next two months, and monthly for months 3-6. Investigators will use the PATHFAST-LAM test to measure LAM levels in sputum and urine. Since there are no previous studies that have evaluated the relationship between sputum LAM and treatment outcome, investigators will do an initial analysis with 30 participants, and based on that, investigators will determine the final number of participants needed for our study.
It is expected that sputum LAM decreases when the treatment is successful and remains positive (does not decrease) when treatment is unsuccessful, with patients experiencing unfavorable results. How LAM decreases during the earlier course of TB treatment may be useful in predicting patients' outcomes. The results of this study could provide a faster and effective way for monitoring TB treatment. This could contribute to improved patient outcomes and help reduce the global burden of TB.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Pulmonary Tuberculosis Patients
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients with a recent diagnosis of bacteriologically confirmed PTB who have not yet initiated TB treatment.
* Patients who are willing and able to visit to the facility for follow-up sample collection and interviews.
* Patients who are willing and able to provide written informed consent to participate in the study.
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Nagasaki University
OTHER
Responsible Party
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Nobuo Saito
Associate Professor
Locations
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Mbagathi County Referral Hospital
Nairobi, , Kenya
Rhodes Chest Clinic
Nairobi, , Kenya
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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KEMRI/SERU/CRDR/124/5241
Identifier Type: -
Identifier Source: org_study_id
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