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OpenTrials
Completed

NCT Number: NCT04718220

Safety, Testing/Transmission, and Outcomes in Pregnancies With COVID-19

Pregnant women are a vulnerable and high-risk population, as COVID-19 is associated with an increased risk preterm birth, cesarean section, and maternal critical care. This study will examine the factors that impede testing for SARS-CoV-2 (the causative virus among pregnant women), help determine optimal testing strategies by evaluating the necessity of testing for asymptomatic disease in pregnancy, inform prenatal care plans by assessing the full impact of infection, and contribute to a provider's ability to counsel women and create prenatal care plans if they are pregnant or considering pregnancy.

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Key information

About this study

Pregnant women are a vulnerable and high-risk population, as COVID-19 is associated with an increased risk of preterm birth, cesarean section, and maternal intensive care. The objectives of this study are to: (a) evaluate the full impact of SARS-CoV-2 in pregnancy to inform testing strategies, (b) examine the factors that impede testing during pregnancy, and (c) use study data to devise implementation strategies that improve SARS-CoV-2 testing in pregnancy and prenatal care during the pandemic. Investigators will prospectively enroll two cohorts of pregnant women: 1) exposed (SARS-CoV-2 positive), and 2) unexposed (SARS-CoV-2 negative as defined by antibody testing at the beginning of pregnancy, every trimester, and at delivery). Women who initially enroll as unexposed but later test positive for SARS-CoV-2 antibodies will cross over to the exposed cohort. In Aim 1, investigators will evaluate patients' and providers' perceptions of SARS-CoV-2 testing during pregnancy and the influence of COVID-19 on maternal care-seeking behavior and anxiety via surveys and semi-structured interviews. In Aim 2, investigators will determine the effect of SARS-CoV-2 infection during pregnancy on the risk of preterm birth and other adverse pregnancy outcomes in symptomatic and asymptomatic disease. It is hypothesized that SARS-CoV-2 infection will increase the risk of preterm birth by 12%. In Aim 3, investigators will estimate the risk of mother-to-fetus SARS-CoV-2 transmission and viral presence in umbilical cord blood, placenta, and amniotic fluid by assaying for viral RNA in the neonate, cord blood, and placenta. Collectively, Aims 1-3 will be interpreted by investigators, the Scientific Advisory Board and the Community Advisory Board who will apply data to devising targeted implementation strategies designed for rapid community dissemination to improve testing and prenatal care.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for exposed (SARS-CoV-2 positive) cohort:

  • Viable intrauterine pregnancy
  • Seroconversion or SARS-CoV-2 IgG antibodies or positive RT-PCR for SARS-CoV-2 during current pregnancy

Exclusion criteria

for exposed (SARS-CoV-2 positive) cohort:

  • No viable intrauterine pregnancy
  • No history of SARS-CoV-2 infection during pregnancy

Inclusion criteria

for unexposed (SARS-CoV-2 negative) cohort:

  • Viable intrauterine pregnancy
  • No history of SARS-CoV-2 infection prior to pregnancy

Exclusion criteria

for unexposed (SARS-CoV-2 negative) cohort:

  • No viable intrauterine pregnancy
  • Detection of SARS-CoV-2 IgG antibodies at enrollment

Treatment and study plan

Antibody testing for SARS-CoV-2 IgG

Diagnostic Test

Women enrolled into the unexposed (SARS-CoV-2 negative) cohort will undergo testing for SARS-CoV-2 IgG antibodies at enrollment, every trimester of pregnancy, and during delivery hospitalization.

Testing for SARS-CoV-2 RNA

Diagnostic Test

Women in the exposed (SARS-CoV-2 positive) cohort will undergo testing of placental tissue, umbilical cord blood, amniotic tissue, and neonates for SARS-CoV-2 RNA, as available.

Testing for SARS-CoV-2 IgM/IgG

Diagnostic Test

Women in the exposed (SARS-CoV-2 positive) cohort will undergo testing of umbilical cord blood for SARS-CoV-2 IgG and IgM antibodies, as available.

Primary outcomes

  1. Rate of preterm delivery

    Time frame: 20 weeks gestation until childbirth

    Childbirth prior to 37 weeks of pregnancy, to be determined in accordance to standard pregnancy dating and the established estimated due date.

Secondary outcomes

  1. Rate of preeclampsia

    Time frame: After 20 weeks gestation and up to 6 weeks postpartum

    Standard definitions will be used (new-onset presence of elevated blood pressure > 140 systolic or > 90 diastolic separated by >4 hours and new onset proteinuria after 20 weeks of pregnancy or evidence of severe features of preeclampsia).

  2. Rate of gestational hypertension

    Time frame: After 20 weeks gestation and up to 6 weeks postpartum

    Standard definitions of gestational hypertension will be used (new-onset presence of elevated blood pressure > 140 systolic or > 90 diastolic separated by >4 hours without proteinuria after 20 weeks of pregnancy).

  3. Rate of cesarean section

    Time frame: Time of delivery

    Delivery via a cesarean section operation.

  4. Rate of stillbirth

    Time frame: Between 20 weeks gestation and childbirth

    Fetal demise in utero after 20 weeks gestation.

  5. Rate of fetal growth restriction

    Time frame: Between conception and childbirth

    Estimated fetal weight by sonographic assessment less than the 10th percentile for gestational age.

  6. Rate of fetal hydrops

    Time frame: Between conception and childbirth

    The presence of abnormally located fluid collections in two or more areas in the fetal body (i.e., fetal ascites and pericardial effusion) or one abnormal fluid collection plus fetal skin thickening.

  7. Rate of oligohydramnios

    Time frame: Between conception and childbirth

    Estimated amniotic fluid index less than 5 or estimated deepest vertical pocket (no presence of umbilical cord) less than 2 by sonographic assessment.

  8. Perinatal death

    Time frame: During the pregnancy after 20 weeks of pregnancy to 21 days after delivery

    Fetal or neonatal death occurring after 20 weeks gestation and up to 21 days of life.

  9. Rate of premature preterm rupture of membranes

    Time frame: Between conception and 36 weeks 6 days of pregnancy

    Rupture of membranes prior to 37 weeks gestation.

  10. Rate of neonatal intensive care unit (NICU) admission

    Time frame: After delivery of newborn during delivery hospitalization

    Admission of the newborn to the NICU after delivery during delivery hospitalization.

  11. Rate of neonatal sepsis

    Time frame: After delivery of newborn during delivery hospitalization up to 6 weeks of life

    Clinical syndrome that includes systemic signs of infection and bacteremia.

  12. Rate of oxygen therapy

    Time frame: After delivery of newborn during delivery hospitalization up to 6 weeks of life

    Use of oxygen therapy for the newborn after delivery during delivery hospitalization.

  13. Percentage of infants with low 5-minute Apgar

    Time frame: At time of delivery

    Five minute Apgar less than 7. Maximum 10, minimum 0. Higher scores typically have improved outcomes.

  14. Percentage of infants with abnormal umbilical cord gas

    Time frame: At time of delivery

    pH of arterial blood of umbilical cord blood less than 7 and/or base excess greater than -12.

  15. Low birth weight

    Time frame: At time of delivery

    Weight at birth less than 2,500 grams.

  16. Confirmed congenital infection

    Time frame: Testing will be conducted at time of delivery.

    SARS-CoV-2 RNA detection in the umbilical cord blood, in amniotic fluid if collected before rupture of membranes or in neonatal nasopharyngeal swabs collected both immediately after birth (and after cleaning of the infant).

  17. Probable congenital infection

    Time frame: At time of delivery

    SARS-CoV-2 RNA detection in the neonatal nasopharyngeal swabs collected immediately after birth (after cleaning of infant) and in the fetal side of the placenta.

  18. Possible congenital infection

    Time frame: At time of delivery

    Anti-SARS-CoV-2 IgM antibodies detection in the umbilical cord blood but no SARS-CoV-2 RNA detected in the neonate.

Sponsors and collaborators

Lead sponsor

Washington University School of Medicine

Other

Collaborators

  • Mercy Research

Registry information

Acronym: STOPCOVID19

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Jan 22, 2021
Registry last updated
Apr 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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