Coronavirus Disease 2019 (COVID-19) During Pregnancy: Prevalence of Seroconversion, Effect on Maternal and Perinatal Outcomes and Risk of Vertical Transmission (COVID-MAP)

NCT04465474 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2024-02-08

No results posted yet for this study

Summary

The objectives of this proposal are to: 1) determine the rate of SARS-CoV-2 seroconversion in unselected pregnant women in Hong Kong; 2) determine the rate of SARS-CoV-2 infection in women presenting with miscarriage and stillbirth; 3) follow the pregnancy course and perinatal outcome of confirmed COVID-19-infected pregnant cases; 4) determine the risk and characteristics of vertical transmission; and 5) evaluate the placental barrier, immune response and fetal damage in vertical transmission of SARS-CoV-2. A series of longitudinal and cross-sectional observational studies, and a laboratory-based study will be conducted to fulfil the 5 objectives.

Conditions

Interventions

OTHER

Non Intervention

It's an observational study, no intervention involves.

Sponsors & Collaborators

  • Peking University First Hospital

    collaborator OTHER
  • Hospital Universitario de Torrejón

    collaborator UNKNOWN
  • Queen Mary Hospital, Hong Kong

    collaborator OTHER
  • Pamela Youde Nethersole Eastern Hospital

    collaborator OTHER
  • Queen Elizabeth Hospital, Hong Kong

    collaborator OTHER
  • United Christian Hospital

    collaborator OTHER
  • Kwong Wah Hospital

    collaborator OTHER
  • Princess Margaret Hospital, Hong Kong

    collaborator OTHER_GOV
  • Tuen Mun Hospital

    collaborator OTHER_GOV
  • Chinese University of Hong Kong

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-05-01
Primary Completion
2024-04-30
Completion
2024-12-31

Countries

  • China
  • Hong Kong
  • Spain

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04465474 on ClinicalTrials.gov