Burden of Tuberculosis Among Pregnant and Postpartum Women in Guinea-Bissau

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15+
SponsorAarhus University Hospital

About this trial

This study aims to address critical diagnostic and data gaps in tuberculosis (TB) care among pregnant and postpartum women in Guinea-Bissau, a high-burden, resource-limited setting. Recognising that current TB screening during antenatal care (ANC) relies largely on unstructured symptom questions, the study will integrate more systematic and innovative approaches into routine maternal health services.

The project will implement the Bandim TBscore II as a structured triage tool to classify symptom severity and guide referrals. To strengthen diagnostic capacity, two novel tools will be evaluated: stool-based GeneXpert testing (a method recommended in children and explored here as a feasible alternative for pregnant women) and artificial intelligence-powered chest X-ray interpretation software designed to enhance TB detection where radiological expertise is lacking.

The study will also generate comprehensive, population-based data on TB and TB infection (TBI) among pregnant, postpartum women and women of reproductive age in Guinea-Bissau. The results are intended to inform health policy, both locally and in high-income countries, by providing evidence to improve TB screening protocols and care for this vulnerable group. Ultimately, the study seeks to develop scalable strategies that can be replicated across low- and middle-income countries to advance maternal and child health and support global TB eradication efforts.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Pregnant women ≥ 15 years of age

Residing in the study

Attending ANC consultations at health centre in Bandim, Belem or Cuntum

Must provide informed consent

Disqualifiers

Pregnant women ≤ 15 years of age

Inability to provide informed consent

Residing outside of the study area

Receives TB treatment at the time of, or a year prior to, enrolment

Trial design

Design model

Sequential

Treatments tested in this trial

  • Enhanced protocol

    Diagnostic test

    In the intervention, and inclusion and subsequent ANC visits, pregnant women will be interviewed by midwives regarding TB exposure and previous TB, and systematically screened with the Bandim TBscore II, which categorises patients based on the severity of their symptoms. Women exhibiting moderate symptoms (TBscoreII=2-3) suggestive of TB will be referred for GeneXpert testing sputum and/or faecal samples, while individuals with more severe symptoms (TBscoreII=4-8) will additionally receive chest radiography, which will be analysed with AI software. Due to high co-infection rates, all HIV-positive women, regardless of their Bandim TBscore II, will be tested with both GeneXpert and chest radiography. Women with positive GeneXpert results will be referred for treatment, while women with chest radiography will attend a consultation with a TB specialist. Participants will be reassessed for TB symptoms at each subsequent ANC visit and at 6 months postpartum.

Treatment groups

720 Participants
are divided into 2 treatment groups
Group A: BaselineNo intervention 0 interventions
Group B: Intervention (Enhanced protocol)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Number of active TB cases

Number of number of bacteriologically or radiologically confirmed active TB cases comparing baseline and intervention (enhanced protocol)

Time frame
From enrolment to 6 months postpartum

Secondary outcomes

1

TBI prevalence

Number of pregnant women with confirmed TBI

Time frame
At enrolment
2

Progression from TBI to active TB disease

Number of women which develop active TB disease during pregnancy or postpartum period

Time frame
From enrolment to 6 months postpartum

Other outcomes

Sponsors and contacts

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Aarhus University Hospital

Lead sponsor

Bandim Health Project

Collaborator

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