ClinicalTrials.gg
CompletedNCT03305991Updated Mar 13, 2024

Tuberculosis Infection in Women of Reproductive Age and Their Infants

An observational study in Tuberculosis and Pregnancy Complications, sponsored by Lund University. Completed at 3 sites in Ethiopia. Open to female participants. Per ClinicalTrials.gov, last updated 2024-03-13.

Sponsored by Lund University · Observational

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
2,120
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 22 studies in Tuberculosis with a site in Ethiopia — 4 open to participants now, 5 under way, 1 of them phase 3. Tuberculosis · Ethiopia.

Started
2015
the only one that year
Observational
8 of 22
1 open now
Registered
9th of 22
by date
Lead sponsor
4 of 22
Lund University

Among the 22 studies in Tuberculosis with a site in Ethiopia, this one is the only one that started in 2015, is one of 8 observational ones, and was the 9th registered.

Tuberculosis

1,170 studies on the registry are indexed under Tuberculosis; 175 are open to participants now.

Browse Tuberculosis studies →

Open to participants now

4 of the 22 studies in Tuberculosis with a site in Ethiopia are open now. Recruiting first, the newest first:

All 4 open studies →

A study can be open while its sites in Ethiopia have not opened yet or have stopped. Only those recruiting at a site in Ethiopia →

Who these studies take

Of the 111 Tuberculosis studies recruiting now, 65 (59%) set no upper age limit and 36 (32%) stop at 75 or younger; 48 take children under 18; 31 take healthy volunteers.

This study: female · no healthy volunteers.

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02

Study summary

Women living in low-income countries are at elevated risk of death in connection to pregnancy, as well as infants born to women in such settings. It is probable that several factors are involved, such as poverty, lack of education and access to healthcare. Infectious diseases constitute important threats to maternal health in resource-limited settings. Tuberculosis (TB) is reported to be the third leading cause of maternal death globally. Furthermore, TB can be transmitted from mother to child during pregnancy, with high risk of severe consequences for the infant. Despite these data, neither the role of TB in relation to co-existing risk factors for adverse pregnancy outcomes, nor the mechanisms involved, are well understood. It is likely that TB interacts with other characteristics, in particular socio-economic condition and HIV infection, which could obscure associations between TB and pregnancy outcomes. For this reason, it is critical to design studies so that the independent role of TB can be deduced.

This project aims to investigate how TB infection in women affects the risk of adverse pregnancy outcomes in relation to co-existing factors, and how exposure to TB infection may impact growth and development of infants born to women with TB. In addition, mechanisms in which TB and the immune system during pregnancy will be explored.

The project is conducted at public health facilities in Ethiopia, where 2 000 women have been recruited during antenatal care. These women will be followed until 5 years after delivery, along with their offspring born during the study period. Detailed data is collected at inclusion and at study visits during follow-up, with submission of samples for TB testing and immunological analyses.

Better knowledge on the characteristics of TB infection in association with pregnancy, and how TB affects maternal and child health, can be used to construct new guidelines for management of TB in women of fertile age. This may contribute to reductions in adverse pregnancy outcomes, including maternal and infant deaths.

Read the detailed description

Objective The overall objective of this project is to investigate longitudinal patterns and consequences of tuberculosis (TB) infection in a prospective cohort of women recruited during pregnancy. The relation between maternal TB infection and pregnancy outcomes, as well as infant health and development, will be evaluated over time.

Specific aims

  1. To determine whether maternal TB infection is associated with adverse pregnancy outcomes
  2. To determine the excess risk of incident active TB during pregnancy and post-partum, with regard to the prevalence of latent TB infection at registration in antenatal care
  3. To investigate long-term health and survival in infants in relation to maternal TB and adverse pregnancy outcomes

Methods Study setting and participants This project is conducted in public health facilities in the city of Adama, Central Ethiopia. Participants are recruited and followed at antenatal care (ANC) clinics until delivery. After delivery their children are followed at clinics for extended program for immunization (EPI); continued follow-up of the mothers after the first post-natal visit also takes place in these clinics.

All study procedures, including interviews, physical examination, and collection of informed consent, are performed by health facility staff (nurses and midwives) in the respective clinics. Biological samples including blood and sputum are collected at the respective health facility laboratory. Study samples are transported to the Adama Regional Laboratory. At this laboratory, additional analyses and storage of plasma will be done.

For supervision and monitoring of data collection, as well as for data entry, the project uses staff and infrastructure in a field research station which has been established in Adama since 2010 by the research group.

Study procedure Both scheduled and unscheduled study visits can occur for participants in this project. Scheduled study visits coincide with routine antenatal and postnatal visits and visits at the EPI clinics for the infant's immunization following National guidelines. Unscheduled visits occur in case of symptoms suggestive of active TB (according to the study definitions) in the pregnant/postnatal/non-pregnant woman, or in the child, at any time in between these routine visits.

Antenatal care visits At inclusion, structured information on socio-demographic conditions, education, occupation, and poverty indicators is collected; as well as medical history (in particular for obstetric, gynecological and TB-related details). Physical and obstetric examination is performed. Apart from the study procedures and investigations, participants will receive care according to current Ethiopian ANC guidelines.

At the inclusion visit blood samples are obtained for routine care and for study specific investigations from all participants. At the health facility laboratory, the following analyses are performed: HIV rapid test, urine dipstick. Ten mL of venous blood is collected. This sample is used for analysis of complete blood count, blood/Rh group, syphilis serology, creatinine and fasting glucose. The remaining plasma is aliquoted and stored at -80° C for research analyses that are performed at the completion of inclusion. Blood is collected separately for QuantiFERON TB Plus (QFT) testing, in order to determine the prevalence of LTBI. For the last 500 women included in the study, QFT testing is repeated at the 3rd antenatal care visit. From HIV positive women blood for viral load and CD4 count is drawn at each scheduled visit pre- and post-delivery except from 2nd and 3rd antenatal care visit.

Participants are followed up four times in accordance with WHO recommended focused antenatal visits until delivery or term of pregnancy. They are also instructed to contact the study clinic in between these visits in case of health-related events. In case of delivery (or other unintended termination of pregnancy) in another place than any of the study health facilities, they are asked to communicate this to their study site for further follow-up examinations.

All participants with suspected active TB according to the study definition (irrespective of Quantiferon results) at enrolment and/or during follow up are asked to submit samples for bacteriological TB investigations. These encompass liquid culture, smear microscopy and PCR (using Xpert MTB/RIF technique). All these tests are performed on two consecutive morning sputum samples. Moreover, acquisition of blood for QuantiFERON testing is repeated for all women investigated for suspected active TB.

Stored aliquots of Mtb-incubated plasma will be analyzed at the end of inclusion for potential blood biomarkers of TB infection during pregnancy. These analyses will be performed using ELISA and/or Luminex technique, and they will include the following markers of immune activation and inflammation: C-reactive protein (CRP), neopterin, soluble urokinase-plasminogen activator receptor (suPAR), interferon-inducible protein 10 (IP-10).

Postpartum follow-up visits for women Further follow-up visits for women are scheduled for 6 weeks and 9 months after delivery or termination of pregnancy, coinciding with the routine child visits for immunization. The first postnatal visit takes place at the ANC clinic, whereas all subsequent visits take place at the respective EPI clinics (where infant follow-up also occurs). At the 6 week postnatal visit details on delivery outcome are recorded.

For investigation of long-term health effects after delivery, participants will be asked to come for further annual visits with similar assessments until 54 months after termination of pregnancy. At all follow-up visits symptoms and signs on physical examination will be recorded using structured questionnaires.

At inclusion, and repeatedly on scheduled follow-up visits, participants are informed about symptoms and signs that may indicate active TB. Study subjects are instructed to contact the study site clinic (ANC during antenatal period, EPI during postnatal period) directly if they develop such symptoms for unscheduled study visits (in order to assess incident active TB during follow-up).

At all visits, whether scheduled or unscheduled, bacteriological testing (smear microscopy, Xpert MTB/RIF assay, and liquid culture) is performed according to the study protocol in case study criteria for suspected active TB are met. These tests are performed on two morning sputum samples.

In case study participants do not come for their scheduled study visits they are contacted by phone by the study site staff and/or the research study team. If the participant cannot be reached, her contact person is contacted by phone. At mid-time in between the scheduled visits, women are contacted by phone by a member of the local research team to assess whether any health events or symptoms compatible with TB have occurred.

Repeated sampling for QFT testing will be performed for all women at 4 years after inclusion (irrespective of previous QFT results), with storage of incubated plasma for further analysis of immune markers of TB infection.

Follow-up visits for infants If consent has been provided by the mother, infants are registered and included in a separate infant follow-up cohort as soon as possible after birth. Birth details, including delivery method, weight, length, APGAR score, and head circumference are registered at inclusion of the infant. Follow-up of included infants takes place in the EPI clinic at the respective study health facilities. Follow-up visits are scheduled at the same time interval as the mother, i.e. at 6 weeks and 9 months and subsequently at annual intervals congruent with the mothers until four and a half year after birth. The two first visits coincide with routine immunization visits. On all study visits, parameters of growth, nutritional and neurological development are recorded using structured questionnaires. In addition, data on socio-demographic characteristics, health-related events and feeding details are recorded, as well as data on known or suspected exposure to TB.

At inclusion, and repeatedly on scheduled follow-up visits, caretakers are informed about symptoms and signs that may indicate active pediatric TB. Study infant caretakers are instructed to contact the study site EPI clinic directly if the infants develop such symptoms for unscheduled study visits (in order to assess incident active TB during follow-up).

If criteria for suspected TB are met at any time during follow-up bacteriological investigations (liquid culture, PCR and microscopy) will be performed on gastric lavage specimens (or cerebrospinal fluid in case of suspected meningitis; or fine-needle lymph node aspirates in case of peripheral lymphadenopathy). These investigations will be performed by trained health care staff at the Department of Pediatrics, Adama Regional Hospital.

Stored aliquots of plasma will be analyzed at the end of inclusion for potential blood biomarkers of TB in young children. These analyses will be performed using ELISA and Luminex technique, and they will include the following markers of immune activation and inflammation: C-reactive protein (CRP), neopterin, soluble urokinase-plasminogen activator receptor (suPAR).

In case infant participants do not come for their scheduled study visits their caretakers are contacted by phone by the study site staff and/or the research study team. If the caretaker cannot be reached, the contact person is contacted by phone. At mid-time in between the scheduled visits, caretakers are contacted by phone from a study investigator to assess whether any health events or symptoms compatible with TB have occurred in the infant.

Study definitions Suspected adult active TB is defined as any of the following symptoms or findings: Cough, fever, night sweating, weight loss (except following delivery), chest pain, reduced Karnofsky performance score (after pregnancy), peripheral lymph node enlargement, abdominal distension and/or abdominal mass (during study periods without pregnancy).

Suspected pediatric active TB is defined as any of the following symptoms or findings: Cough, fever, night sweating, chest pain, peripheral lymph node enlargement, abdominal distension and/or mass, weight loss, poor growth development, failure to thrive, acute or chronic malnutrition, neck stiffness, seizures, and loss of consciousness Latent TB infection is defined as a positive QuantiFERON® TB Gold Plus result (according to the manufacturer's reference range), in the absence of confirmed active TB and/or national TB guideline criteria for clinically diagnosed TB.

Confirmed active TB is defined as any subject with a positive bacteriological result (as per the national TB guideline), irrespective of clinical manifestations.

Clinically diagnosed active TB is defined as any subject without positive bacteriological results for TB, but who fulfils national TB guideline criteria for clinically diagnosed TB, and who are referred for anti-TB treatment.

Adverse pregnancy outcomes are defined as maternal or infant death following inclusion until 3 months after unintended termination of pregnancy; preterm birth (before 37 gestational weeks); spontaneous abortion; PE (as defined by the International Society for the Study of Hypertension in Pregnancy; 25); IUGR; peri-partum hemorrhage.

Intra uterine growth restriction is defined as growth deviation of weight below 2 SD (-22% or below 3rd quartile) at birth.

Post-partum TB is defined as confirmed or clinically diagnosed active TB within the 6 months period following termination of pregnancy.

03

Conditions studied

  • Tuberculosis
  • Pregnancy Complications

Keywords

  • tuberculosis
  • pregnancy
  • ethiopia
04

Who can participate

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

Study population

Participants are identified at antenatal care clinics at three public health facilities. The study population consists of women of reproductive age who are identified and recruited in antenatal care and followed until delivery and 4 years post-partum. Children born to participants of the study are followed for 4 years after birth for assessment of survival, growth and development.

Inclusion criteria

  • Pregnant women attending antenatal care at any of the study facilities
  • First antenatal care visit for current pregnancy
  • Written
  • Accepts testing
  • Residence in uptake area during pregnancy period

Exclusion criteria

Exclusion Criteria:

-

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
2,120 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna
06

What researchers measure

Primary outcomes

  1. Incidence of adverse pregnancy outcomes

    Reports of pregnancy outcomes of participating women, collected and assessed during study follow-up and categorized with regard to normal or adverse pregnancy outcomes

    Time frame: 2015-2023

Secondary outcomes

  1. Incidence of active tuberculosis in participants during pregnancy, post-partum period and periods outside pregnancy, respectively

    Bacteriologically and/or clinically diagnosed cases of active tuberculosis during study follow-up, categorized with regard to timing in relation to pregnancy

    Time frame: 2015-2023

  2. Pattern of child growth with regard to maternal tuberculosis infection status during pregnancy

    Growth curves of children born to participating women, recorded during study follow-up until 4 years of age

    Time frame: 2016-2023

  3. Incidence of tuberculosis infection in Ethiopian infants during the first four years of life

    Latent and active tuberculosis at 4 years of age among children born to women in the study cohort

    Time frame: 2021-2023

07

Study locations

3 sites
  • Adama Health Center
    Adama, Ethiopia
  • Adama Regional Hospital
    Adama, Ethiopia
  • Gheda Health Center
    Adama, Ethiopia
08

References and documents

Publications

  • Getahun H, Sculier D, Sismanidis C, Grzemska M, Raviglione M. Prevention, diagnosis, and treatment of tuberculosis in children and mothers: evidence for action for maternal, neonatal, and child health services. J Infect Dis. 2012 May 15;205 Suppl 2:S216-27. doi: 10.1093/infdis/jis009. Epub 2012 Mar 22. PubMed 22448018 ↗
  • Grange J, Adhikari M, Ahmed Y, Mwaba P, Dheda K, Hoelscher M, Zumla A. Tuberculosis in association with HIV/AIDS emerges as a major nonobstetric cause of maternal mortality in Sub-Saharan Africa. Int J Gynaecol Obstet. 2010 Mar;108(3):181-3. doi: 10.1016/j.ijgo.2009.12.005. Epub 2010 Jan 13. PubMed 20070964 ↗
  • Jana N, Vasishta K, Saha SC, Ghosh K. Obstetrical outcomes among women with extrapulmonary tuberculosis. N Engl J Med. 1999 Aug 26;341(9):645-9. doi: 10.1056/NEJM199908263410903. PubMed 10460815 ↗
  • Mathad JS, Bhosale R, Sangar V, Mave V, Gupte N, Kanade S, Nangude A, Chopade K, Suryavanshi N, Deshpande P, Kulkarni V, Glesby MJ, Fitzgerald D, Bharadwaj R, Sambarey P, Gupta A. Pregnancy differentially impacts performance of latent tuberculosis diagnostics in a high-burden setting. PLoS One. 2014 Mar 21;9(3):e92308. doi: 10.1371/journal.pone.0092308. eCollection 2014. PubMed 24658103 ↗
  • Kothari A, Mahadevan N, Girling J. Tuberculosis and pregnancy--Results of a study in a high prevalence area in London. Eur J Obstet Gynecol Reprod Biol. 2006 May 1;126(1):48-55. doi: 10.1016/j.ejogrb.2005.07.025. Epub 2005 Sep 9. PubMed 16154251 ↗
  • Rustveld LO, Kelsey SF, Sharma R. Association between maternal infections and preeclampsia: a systematic review of epidemiologic studies. Matern Child Health J. 2008 Mar;12(2):223-42. doi: 10.1007/s10995-007-0224-1. Epub 2007 Jun 19. PubMed 17577649 ↗
  • Rowe JH, Ertelt JM, Way SS. Foxp3(+) regulatory T cells, immune stimulation and host defence against infection. Immunology. 2012 May;136(1):1-10. doi: 10.1111/j.1365-2567.2011.03551.x. PubMed 22211994 ↗
  • Espinal MA, Reingold AL, Lavandera M. Effect of pregnancy on the risk of developing active tuberculosis. J Infect Dis. 1996 Feb;173(2):488-91. doi: 10.1093/infdis/173.2.488. PubMed 8568319 ↗
  • Whittaker E, Kampmann B. Perinatal tuberculosis: new challenges in the diagnosis and treatment of tuberculosis in infants and the newborn. Early Hum Dev. 2008 Dec;84(12):795-9. doi: 10.1016/j.earlhumdev.2008.09.005. Epub 2008 Sep 27. PubMed 18823726 ↗
  • Bekker A, Du Preez K, Schaaf HS, Cotton MF, Hesseling AC. High tuberculosis exposure among neonates in a high tuberculosis and human immunodeficiency virus burden setting. Int J Tuberc Lung Dis. 2012 Aug;16(8):1040-6. doi: 10.5588/ijtld.11.0821. Epub 2012 Jun 12. PubMed 22691968 ↗

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Dec 2015 to primary completion in Mar 2024, 99 months.

Of 123 non-industry observational studies under Tuberculosis, half reached primary completion within 41 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 76. This study's 99 months is above that.

Counting every sponsor, half of 135 studies reached it within 36 months; a quarter within 21 and three quarters within 76.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 2, 2017
First posted
Oct 10, 2017
StartActual
Dec 1, 2015
Primary completionActual
Mar 12, 2024
CompletionActual
Mar 12, 2024
Last update
Mar 13, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 13, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03305991
Lead sponsor
Lund University
Responsible party
Per Bjorkman (Professor, Lund University) — Principal investigator
First posted
Oct 10, 2017
Start date
Dec 1, 2015
Primary completion
Mar 12, 2024
Completion
Mar 12, 2024
Last update
Mar 13, 2024

Study contacts

Per Bjorkman, MD, PhD
principal investigator · Lund University

Oversight

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

Not currently enrolling

This study is completed, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.

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