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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05303168
Other study ID # RIA2020EF-2956
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 1, 2021
Est. completion date May 31, 2024

Study information

Verified date March 2024
Source Barcelona Institute for Global Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

There is growing evidence that COVID-19 threatens maternal and perinatal health. Pregnant women are at higher risk of severe complications (severe pneumonia, hospitalizations, intensive care unit admission, invasive mechanical ventilation, extracorporeal membrane oxygenation) and death compared to age-matched non-pregnant women. On the other hand, the number of confirmed COVID-19 cases reported in sub-Saharan Africa (SSA) continues to increase, where the highest maternal mortality rates in the world are registered. The World Health Organization (WHO) estimates that this region alone accounted for roughly two-thirds (196 000) of all maternal deaths in 2017, which among other reasons is explained by the inequalities in access to quality antenatal care (ANC) services and the low numbers of skilled health workers in the region. The spread of SARS-CoV-2 in SSA is threatening the already fragile health services, affecting mainly the most vulnerable populations such as pregnant women. This project aims to describe the burden and effects of SARS-CoV-2 infection during pregnancy in women living in malaria endemic areas and high prevalence of HIV infection. Pregnant women attending ANC clinics in selected sites from Libreville and Lambaréné (Gabon) and Manhiça (Mozambique) will be enrolled in a cohort study to determine the frequency of SARS-CoV-2 infection and COVID-19 during pregnancy and its effects on maternal and neonatal health. Participants will be tested for SARS-CoV-2 infection whenever reporting respiratory symptoms suggestive of COVID-19 during routine ANC follow-up and six weeks after the end of pregnancy. The presence of antibodies (IgG/IgM) against SARS CoV-2 in blood samples will be determined. The clinical presentation of COVID-19 in pregnancy will be also characterised, and the incidence of infection during pregnancy and the risk factors of maternal and neonatal morbidity and mortality associated with SARS-CoV-2 infection and the frequency of mother- to- child transmission of SARS-CoV-2 will be assessed. The findings of this project will contribute to the understanding of the impact of SARS-CoV-2 and COVID-19 among pregnant women living in SSA countries where malaria and HIV infections are highly prevalent.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1000
Est. completion date May 31, 2024
Est. primary completion date July 5, 2023
Accepts healthy volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Permanent resident in the study area - Agreement to deliver in the study site's maternity(ies) wards Exclusion Criteria: - Planning to move out the study area in the following 7 months from enrolment

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Gabon Centre de Recherches Médicales de Lambaréné (CERMEL) Lambaréné
Mozambique Centro de Investigação em Saúde de Manhiça (CISM) Manhiça

Sponsors (5)

Lead Sponsor Collaborator
Barcelona Institute for Global Health Bernhard Nocht Institute for Tropical Medicine, Centre de Recherche Médicale de Lambaréné, Centro de Investigação em Saúde de Manhiça, Universität Tübingen

Countries where clinical trial is conducted

Gabon,  Mozambique, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of antibodies (Ig G and/or Ig M positive) against SARS-CoV-2 among pregnant women at delivery 7 months
Secondary Incidence of SARS-CoV-2 infection during pregnancy 7 months
Secondary Maternal and neonatal morbidity due to SARS-CoV-2 infection during pregnancy 7 months
Secondary Maternal and neonatal mortality due to SARS-CoV-2 infection during pregnancy 7 months
Secondary Prevalence of pregnancy and perinatal adverse outcomes 7 months
Secondary Rate of vertical transmission of SARS-CoV-2 from infected mothers to their offspring, during the prenatal and perinatal period 7 months
Secondary CD4 cell counts 7 months
Secondary HIV viral load 7 months
Secondary Frequency of malaria parasitaemia at delivery (from maternal sample collected at delivery) 7 months
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