Skip to content

impact of MPXV infection on pregnancy outcome and newborn health

Impact of MPXV infection on pregnancy outcome and newborn health

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202501896590961
Enrollment
150
Registered
2025-01-31
Start date
2024-09-15
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Mpox Pregnancy and Childbirth

Interventions

routine care

Sponsors

Catholic University of Bukavu
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnancy status: all women confirmed to be pregnant at the time of recruitment. Age: women of all ages (assent to be asked for non-legal age to allow for the mother-child pair to benefit from earlier diagnosis, close monitoring, and other advantages the study might offer). Geographical inclusion: residing within the catchment areas of the selected healthcare facilities in South Kivu to ensure that they are likely to continue receiving follow-up care at the participating sites throughout their pregnancy. Symptomatic and asymptomatic participation: Symptomatic: pregnant women presenting with symptoms suggestive of Mpox, such as fever, rash/skin lesion, and/or lymphadenopathy. Asymptomatic: pregnant women attending routine antenatal visits who do not exhibit Mpox-related symptoms but are screened as part of the study's surveillance efforts or who report a confirmed case of Mpox in the household/or among closed contacts Consent: women who provide written informed consent to participate in the study, having understood the purpose, procedures, potential risks, and benefits of the study.

Exclusion criteria

Exclusion criteria: 1. Non-consent: pregnant women who do not consent/or their parent-caregiver to participate in the study. 2. Plans to relocate: women who plan to move out of the geographical study area during the study period, which would interfere with follow-up. 3. Participation in other studies: women currently participating in other studies (such as clinical trials) that might interfere with the results of this study, especially trials involving new experimental treatments for Mpox or other infectious diseases.

Design outcomes

Primary

MeasureTime frame
The incidence of MPVX infection during pregnancy and associated adverse outcomes, such as spontaneous miscarriage, stillbirth, and preterm delivery.

Secondary

MeasureTime frame
Immunological responses to infection and vaccination, as well as histopathological findings in the placenta of infected mothers.

Countries

Democratic Republic of the Congo

Contacts

Public ContactWyvine Bapolisi

Postdoc researcher

bawiansi@gmail.com+243852444993

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026