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Saliva and Dried Blood Spot Therapeutic Drug Monitoring for MDR-TB in Tanzania

Saliva and Dried Blood Spot Therapeutic Drug Monitoring for MDR-TB in Tanzania

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04124055
Enrollment
51
Registered
2019-10-11
Start date
2019-09-24
Completion date
2019-12-31
Last updated
2020-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

MDR-TB

Brief summary

Dried blood spot and saliva samples are collected during multidrug resistant tuberculosis (MDR-TB) treatment to measure the drug concentration of levofloxacin. Feasibility of both analytical procedures in a high burdened setting is explored.

Detailed description

Background: Measuring pharmacokinetic variability of anti-tuberculosis (TB) drugs and responding by dose correction will allow individualized treatment to improve microbiological response, curb acquired drug-resistance, protect and extend the efficacy of novel drugs rolled-out to endemic areas (pharmacovigilance), reduce toxicity to patients and lead to treatment duration shortening. Aims and Objectives: Implement Dried Blood Spot (DBS) collection for performance of high-performance liquid chromatography (HPLC) to optimize multidrug resistant TB (MDR-TB) treatment in Tanzania. Simultaneously, provide a proof-of-principle-demonstration that the developed saliva point of care drug assay for measurement of fluoroquinolone concentration works in a field setting. Methods: This will be a phase II prospective diagnostic study among patients from a national referral of MDR-TB in Tanzania. The investigators anticipate recruiting a minimum of 50 study participants to power for the primary aim. Subjects will have a minimum amount of blood and saliva collected for therapeutic drug monitoring and the investigational drug assays respectively. Expected results include agreement of saliva point-of-care and DBS for measurement of fluoroquinolone concentrations in HPLC. Other important findings related to field-testing include the best time for sample collection within the dosing interval and the algorithmic use of DBS and saliva, and clinical - demographic factors such as HIV coinfection, concomitant drugs, and diabetes mellitus that may influence the saliva drug assay results. Performance characteristics (sensitivity, specificity, negative and positive predictive values) of the saliva point-of care (PoC) and DBS will be calculated as a measurement of accuracy with reference to the gold standard.

Interventions

Saliva and dried blood spot samples are collected. Based on the measured drug concentration the dose can be adjusted

Sponsors

Kibong'oto Infectious Diseases Hospital
CollaboratorOTHER_GOV
University of Virginia
CollaboratorOTHER
Jan-Willem C Alffenaar
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Participant is receiving care at Kibong'oto hospital * Age of 18 years or above

Exclusion criteria

* Pregnancy at any gestation * Co-morbid conditions such as generalized severe ulcers, Kaposi sarcoma, * Hemophilia * Participants with medical conditions like malignancy, dementia or those who will be critically ill and unable to consent and provide DBS and Saliva. * Patients with Karnofsky score less than 40% or moribund

Design outcomes

Primary

MeasureTime frameDescription
Drug exposure>2 weeks on treatmentDrug concentration (mgL)

Countries

Tanzania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026