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RecruitingNCT05022238H3TBUpdated Oct 24, 2024

Hotspots, Households and Hospitals: Enhanced Drug-resistant Tuberculosis Case Finding in Namibia

An observational study in Tuberculosis, Multidrug-Resistant, sponsored by University of Namibia. Recruiting at 1 site in Namibia. Per ClinicalTrials.gov, last updated 2024-10-24.

Sponsored by University of Namibia · Observational

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year 1 month ago, but the record still lists the study as recruiting.
  • Started Aug 2022; still recruiting 4 years 2 months later.
Study type
Observational
Model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
2,100
Sex
All
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Study summary

Poor case management, pharmacokinetic variability and on-going transmission have fostered the drug-resistant tuberculosis (DR-TB) epidemic leading to a global estimated number of >500,000 new multidrug resistant (MDR) TB cases per year, of which roughly 10% are extensively drug resistant (XDR). Namibia is a high TB burden country with an incidence rate of 446/100,000 in 2016; about 11,000 new cases per year. 3.9% of new cases and 8.7% of previously treated cases have MDR-TB. Whole genome sequencing (WGS) has recently been applied to interrogate the complete genetic code of Mycobacterium tuberculosis (Mtb) strains. WGS can be used to infer relationships between identified strains as well as determine genomic variations involved in resistance development.

The specific aims of the H3TB study are to: (i) characterise the DR-TB epidemic, in terms of clinical, epidemiological, geospatial, social network and laboratory data, to identify transmission hotspots in three regions of Namibia, (ii) evaluate the feasibility of targeted case finding intervention strategies to improve DR-TB control in highly affected populations and (iii) develop a transmission model to investigate the potential impact of the case finding intervention strategies on DR-TB incidence in Namibia.

A prospective surveillance study started in January 2020, which includes all DR-TB cases in Namibia, and which will nest H3TB. Data collection tools and other study implementation tools have been designed and implemented. The study team is working in close collaboration with the National Institute of Pathology, where all DR-TB cases from the country are registered, to ensure all possible cases are captured. This is important for the identification of transmission hotspots.

After HREC and MOHSS approval, individuals with GeneXpert® MTB/RIF rifampicin-resistant samples and a positive Mtb culture from three regions in Namibia will be included in a transmission hotspot identification study. Preliminary data have shown that DR-TB clusters exist in these regions. Clinical, epidemiological, geospatial, social network and laboratory data (GeneXpert® MTB/RIF, culture, drug sensitivity tests) will be collected. WGS capacity has been established at the UNAM research laboratory, where WGS will be performed on the samples of H3TB participants; results will be validated at the Research Center Borstel in Germany. These study results in conjunction with a systematic review and meta-analysis will inform the design of case finding interventions which will be evaluated through a mixed-methods feasibility study conducted at high transmission areas (hotspots, households and hospitals). Data from these studies and the TB programme will be used to develop the model which will include a health economics component.

The study will strengthen DR-TB diagnosis, surveillance and control, inform DR-TB case finding policy in Namibia and regionally, inform resource allocation by identifying high transmission areas and create preliminary data to design a large scale DR-TB case finding intervention.

02

Conditions studied

  • Tuberculosis, Multidrug-Resistant

Keywords

  • case-finding
  • Namibia
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In context

Tuberculosis

1,417 studies on the registry are indexed under Tuberculosis; 208 are open to participants now.

This study's planned enrollment of 2,100 is above the median of 250 across 421 observational studies indexed under Tuberculosis.

Browse Tuberculosis studies →

Lead sponsor

University of Namibia is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

For the first outcome, the study population is all DR-TB cases in three regions of Namibia, diagnosed by the National Institute of Pathology (GeneXpert Ultra Rifampicin resistant) over 18 months.

For the second outcome, all household contacts of DR-TB cases in the three regions is the study population, as well as DR-TB patients' hospital visitors and community members at transmission hotspots.

Inclusion criteria

  • All cases diagnosed with drug-resistant TB in Namibia, in three regions of Khomas, Otjozondjupa and Ohangwena will be included for the first outcome. For the second outcome, all household members of DR-TB cases will be included; all hospital visitors to DR-TB cases will be included and community members at transmission hotspots will be included.

Exclusion criteria

Exclusion Criteria:

  • Anyone who does not give consent to participate.
05

Study design

Observational model
Ecologic or community
Time perspective
Cross-sectional
Enrollment
2,100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Identification of drug-resistant tuberculosis transmission hotspots in Namibia

    Finding DR-TB transmission hotspots through whole genome sequencing (WGS), social network and shared space analyses, and geospatial analyses. WGS, social network and shared space data, and geospatial data, will be triangulated to identify transmission hotspots.

    Time frame: 18 months

  2. Feasibility study of three interventions to enhance drug-resistant TB case finding in Namibia, measured with a questionnaire

    Evaluating the acceptability, yield and cost of three interventions, viz., finding cases in community transmission hotspots, in drug-resistant tuberculosis hospitals, and in households of drug-resistant tuberculosis patients, in three regions of Namibia

    Time frame: 24 months

  3. Transmission model

    Using programmatic and data from outcomes 1 and 2 to develop and calibrate transmission model to look at the impact of scale-up of interventions

    Time frame: 12 months

07

Study locations

1 of 1 sites recruiting
  • University of Namibia
    Windhoek, Namibia
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — Data will be shared after the acceptance for publication of the main findings from the final dataset by researchers' efforts if a data transfer agreement is made between the custodians of the data (the H3TB study team) and other researchers, that: (i) data will be used only for research purposes, (ii) proper technological measures will be used to ensure data security, (iii) no effort will be made to identify study participants, (iv) data will be destroyed after the agreed analyses and (v) the data source will be acknowledged. The sequencing data will be made available on ReSeqTB or a similar platform. The other data will be stored locally at UNAM in a tailored database and made available by researchers' efforts. These data include individual-level information on health status (e.g., TB and HIV infection status) which cannot be made publicly available.

Supporting information: Study protocol, Sap, Icf

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 24, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05022238
Lead sponsor
University of Namibia
Collaborators
UK Medical Research Council (MRC), European and Developing Countries Clinical Trials Partnership (EDCTP), Research Center Borstel, Imperial College London, University of Stellenbosch, National Taiwan University, Namibian National Tuberculosis and Leprosy Programme (NTLP), UK Foreign, Commonwealth & Development Office (FCDO)
Responsible party
Mareli Claassens (Associate research professor, University of Namibia) — Principal investigator
First posted
Aug 26, 2021
Start date
Aug 1, 2022
Primary completion
Sep 2025 (estimated)
Completion
Sep 2026 (estimated)
Last update
Oct 24, 2024

Study contacts

Mareli Claassens, PhD
Contact
mclaassens@unam.na
264814482082
Mareli Claassens, PhD
principal investigator · University of Namibia

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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