covid19 InfectionCoropregNCT04463758
Covid-19 in Pregnancy: a French Population-based Cohort of Women and Newborns
An observational study of covid19 Infection and Pregnancy Complications, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
The purpose of this study is to characterize the incidence and clinical features of the maternal COVID 19 infection, as well as the associated morbidity of the mother and the child, in the French context Read more about this study
- Who is it for?
- Any age, women only
- Conditions the study is for
- covid19 Infection, Pregnancy Complications, Neonatal Complications
- What is being tested?
- An auto-questionnaire comprising three psychometric scales
- How many people
- 6,015 participants
- Where
- 1 siteFrance
- Study dates
- 11 May 2020to 27 Sep 2022
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- Women only
- No healthy volunteers
- Child, Adult, Older adult
Study population: All pregnant or recently pregnant women managed in one maternity unit of the 16 participating perinatal networks
Who may be able to join
- Any woman with :
- either proven COVID-19 infection= positive PCR test, OR probable COVID-19 infection = typical clinical symptoms AND typical pulmonary radiology
- during pregnancy or within 42 days postpartum,
- whether or not this diagnosis is followed by hospitalization,
Who cannot join
- Refusal to participate
- Major protected (curator, trusteeship)
Trial locations and contacts
1 site in 1 country.
About this study
The purpose of this study is to characterize the incidence and clinical features of the maternal COVID 19 infection, as well as the associated morbidity of the mother and the child, in the French context
Read the detailed description
In the overall context of uncertainty about the morbidity associated with COVID-19 infection and its optimal management, knowledge is urgently required on infection during pregnancy.
First, pregnant women and newborns can have specific and severe reactions to infectious diseases, as seen in previous pandemics which justifies targeted surveillance. Second, optimal management must minimize the health risks of transmission to the newborn. While initial studies did not provide evidence for transmission in utero or during delivery, more recent data suggest that transmission is possible. The virus is present in vaginal secretions and stool, making vertical contamination possible during vaginal delivery. Similarly, transmission may occur during breastfeeding. These risks, which remain theoretical, must be weighed against known harmful consequences of mitigating strategies such as systematic caesarean (increase in maternal morbidity) and separating the child from the mother and contraindicating breastfeeding (negative impact on maternal-child bonding and optimal nutrition). In the absence of reliable data, some maternity hospitals have adopted a maximum precautionary principle, recommending caesarean for all COVID-19 positive women and imposing immediate mother-child separation after childbirth. These approaches are strongly debated in France. Third, optimal management of COVID-19 during pregnancy requires balancing maternal and newborn risks. Risks of maternal deterioration in the event of continuing pregnancy must be weighed against those to the child resulting from indicated preterm birth. This tradeoff is even more complex as evidence-based interventions to protect preterm infants, such as antenatal corticosteroid, may aggravate maternal infection. Finally, childbirth is not an elective procedure and requires managing large numbers of healthy women and newborns in a hospital setting where they are exposed to risks of infection.
Population-based research that captures the diversity of organizational structures and practices within maternity units is needed to guide management during the current epidemic and draw lessons for future infectious pandemics.
Principal innovative features are:
- A population-based approach: Current data systems will include a limited number of pregnant women, principally from university hospitals with specific patient populations and management strategies. Because all maternity hospitals care for COVID-19+ pregnant women, a population-based approach is needed to calculate reliable incidence rates, assess practice variability and measure the impact of differences in management on maternal and newborn infection rates and health.
- The inclusion of infected pregnant women who are not hospitalized and who recover before delivery will provide comprehensive data and measure early fetal in-utero exposure.
- Immediate feedback to clinicians on their practices will inform current controversies about optimal management.
- Joint follow-up of mother and child to 12 weeks after delivery, and longer if indicated, will document the medium-term impact of infection.
- Inclusion of regions with time-varying exposure to the epidemic will provide information to evaluate public health policies.
The results of this study will make it possible to:
- guide care for COVID-19 + mothers and their newborns in real time, through a targeted analysis of key minimum data items, on a bimonthly basis during the epidemic. To achieve this objective, rapid deployment of the data collection system is necessary.
- generate knowledge on the morbidity profile of maternal COVID-19 infection for mother and child, the subgroups at risk, and the impact of management options in real life settings;
- document risks of intrapartum, peri-partum and postpartum transmission based on viral tests performed in the course of routine care; this approach is complementary to the biological collections set up in other projects, which aim to determine the infectious status of pregnant women from specialized centers that are not representative of the general population of pregnant women.
- carry out comparative international research through collaboration with the international INOSS network which is coordinating similar data collection protocols and designs worldwide. The investigators are French INOSS partners.
- evaluate the impact of the epidemic on the organization of care for all pregnant women and newborns. Major and rapid changes to prenatal and childbirth care have been made in response to the epidemic, including spacing out consultations, using teleconsultation instead of in-person visits, restricting the presence of relatives and early discharge. These changes may induce negative consequences, notably delays in the diagnosis of obstetrical complications. It is therefore crucial to document the impact of the epidemic and the resulting measures on the health of all women and newborns. For all pregnant women and newborns monitored in participating maternity hospitals, we will extract routinely collected data from the computerized records of the maternity hospitals and/or via the SNDS-PMSI databases. These data will also be collected for periods before the epidemic to enable comparisons with overall pregnancy outcomes between the two periods. These results can be placed in an international context through collaboration with the European Euro-Peristat network, coordinated by the investigators' research team.
The objective of this multi-regional population-based cohort is to assess the impact of COVID-19 infection during pregnancy on maternal and neonatal health, including rates of perinatal transmission and the influence of diverse management practices on morbidity. The study's focus on this specific population and its population-based coverage complement other facility-based surveillance systems on all cases in France.
- Being tested
- An auto-questionnaire comprising three psychometric scales
- Keywords
- Covid19, Pregnancy, Maternal morbidity, Perinatal mortality, Neonatal morbidity
- Medical subject headings
- COVID-19, Pregnancy Complications, Perinatal Death
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
An auto-questionnaire comprising three psychometric scalesOther
three psychometric scales validated in French: _depression (Edinburgh Postpartum Depression Scale (EPDS)), anxiety (State-Trait Anxiety Inventory (STAI)
- and Impact of Event Scale (Revised) (IES-R)
What is being measured
The primary outcome is the main question the study is designed to answer.
Joint evaluation of morbi-mortality for mother and child up to 12 weeks postpartum
Maternal Criterion: Validated Composite Criterion of Severe Maternal Morbidity (Epimoms study ref 7).
Neonatal Criterion: Mortality and Composite Criterion of Severe Neonatal Morbidity Perinatal asphyxia (arterial pH to cord-7.15 and/or an excess base - 10mmol/L and/or lactates-6 mmol/L, Apgar score at 5 minutes -7), neonatal encephalopathy, seizures, intraventricular hemorrhage, cerebral infarction, periventricular leucomalacia, ulcerative enterocolite, sepsis, respiratory distress syndrome, bronchopulmonary dysplasia, central catheter, ventilatory support, transfusion
Measured: At12 weeks after delivery
Secondary outcomes (3)
Number of women infection COVID-19
Measured: During pregnancy and up to 12 weeks
Severe forms of COVID-19 infection in the mother
Measured: Until 12 weeks after delivery
Severe neonatal morbidity
Measured: Until 12 weeks after delivery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted9 Jul 2020
- Study start11 May 2020
- Primary completion27 Sep 2022
- Study completion27 Sep 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for covid19 InfectionStudies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 6,015 participants (actual)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Collaborators
- INSERM, Epopé team, URC-CIC Paris Descartes Necker Cochin
- Responsible party
- Sponsor
- Investigators
- Pierre Yv Ancel, MD, PhD, Principal investigator, Assistance Publique - Hôpitaux de Paris
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04463758
- Sponsor's protocol ID
- APHP200513
- Acronym
- Coropreg
- Status last verified
- Jun 2026
- First submitted
- 8 Jul 2020
- Last updated
- 1 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Diguisto C, Ancel PY, Seco A, Baunot N, Caze C, Crenn-Hebert C, Dupont C, Garabedian C, Lebeaux C, Le Ray C, Letouzey M, Lorthe E, Marrer E, Rouger V, Vayssiere C, Vauloup Fellous C, Bonnet MP, Deneux-Tharaux C. Incidence, Risk Factors and Outcomes of SARS-CoV-2 Infection in Pregnant Women: The COROPREG Population-Based Study. Paediatr Perinat Epidemiol. 2025 Jul;39(5):477-494. doi: 10.1111/ppe.70028. Epub 2025 May 21.
PubMed 40396221
Study at a glance
From the registry record, last updated by the sponsor on 1 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Covid-19 in Pregnancy: a French Population-based Cohort of Women and Newborns
- ClinicalTrials.gov ID
- NCT04463758
- Acronym / sponsor ID
- Coropreg / APHP200513
- Keywords
- Covid19, Pregnancy, Maternal morbidity, Perinatal mortality, Neonatal morbidity
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 6,015 participants (actual)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Collaborators
- INSERM, Epopé team, URC-CIC Paris Descartes Necker Cochin
- Study start
- 11 May 2020 (actual)
- Primary completion
- 27 Sep 2022 (actual)
- Study completion
- 27 Sep 2022 (actual)
- First posted
- 9 Jul 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to characterize the incidence and clinical features of the maternal COVID 19 infection, as well as the associated morbidity of the mother and the child, in the French context
Detailed description
In the overall context of uncertainty about the morbidity associated with COVID-19 infection and its optimal management, knowledge is urgently required on infection during pregnancy.
First, pregnant women and newborns can have specific and severe reactions to infectious diseases, as seen in previous pandemics which justifies targeted surveillance. Second, optimal management must minimize the health risks of transmission to the newborn. While initial studies did not provide evidence for transmission in utero or during delivery, more recent data suggest that transmission is possible. The virus is present in vaginal secretions and stool, making vertical contamination possible during vaginal delivery. Similarly, transmission may occur during breastfeeding. These risks, which remain theoretical, must be weighed against known harmful consequences of mitigating strategies such as systematic caesarean (increase in maternal morbidity) and separating the child from the mother and contraindicating breastfeeding (negative impact on maternal-child bonding and optimal nutrition). In the absence of reliable data, some maternity hospitals have adopted a maximum precautionary principle, recommending caesarean for all COVID-19 positive women and imposing immediate mother-child separation after childbirth. These approaches are strongly debated in France. Third, optimal management of COVID-19 during pregnancy requires balancing maternal and newborn risks. Risks of maternal deterioration in the event of continuing pregnancy must be weighed against those to the child resulting from indicated preterm birth. This tradeoff is even more complex as evidence-based interventions to protect preterm infants, such as antenatal corticosteroid, may aggravate maternal infection. Finally, childbirth is not an elective procedure and requires managing large numbers of healthy women and newborns in a hospital setting where they are exposed to risks of infection.
Population-based research that captures the diversity of organizational structures and practices within maternity units is needed to guide management during the current epidemic and draw lessons for future infectious pandemics.
Principal innovative features are:
- A population-based approach: Current data systems will include a limited number of pregnant women, principally from university hospitals with specific patient populations and management strategies. Because all maternity hospitals care for COVID-19+ pregnant women, a population-based approach is needed to calculate reliable incidence rates, assess practice variability and measure the impact of differences in management on maternal and newborn infection rates and health.
- The inclusion of infected pregnant women who are not hospitalized and who recover before delivery will provide comprehensive data and measure early fetal in-utero exposure.
- Immediate feedback to clinicians on their practices will inform current controversies about optimal management.
- Joint follow-up of mother and child to 12 weeks after delivery, and longer if indicated, will document the medium-term impact of infection.
- Inclusion of regions with time-varying exposure to the epidemic will provide information to evaluate public health policies.
The results of this study will make it possible to:
- guide care for COVID-19 + mothers and their newborns in real time, through a targeted analysis of key minimum data items, on a bimonthly basis during the epidemic. To achieve this objective, rapid deployment of the data collection system is necessary.
- generate knowledge on the morbidity profile of maternal COVID-19 infection for mother and child, the subgroups at risk, and the impact of management options in real life settings;
- document risks of intrapartum, peri-partum and postpartum transmission based on viral tests performed in the course of routine care; this approach is complementary to the biological collections set up in other projects, which aim to determine the infectious status of pregnant women from specialized centers that are not representative of the general population of pregnant women.
- carry out comparative international research through collaboration with the international INOSS network which is coordinating similar data collection protocols and designs worldwide. The investigators are French INOSS partners.
- evaluate the impact of the epidemic on the organization of care for all pregnant women and newborns. Major and rapid changes to prenatal and childbirth care have been made in response to the epidemic, including spacing out consultations, using teleconsultation instead of in-person visits, restricting the presence of relatives and early discharge. These changes may induce negative consequences, notably delays in the diagnosis of obstetrical complications. It is therefore crucial to document the impact of the epidemic and the resulting measures on the health of all women and newborns. For all pregnant women and newborns monitored in participating maternity hospitals, we will extract routinely collected data from the computerized records of the maternity hospitals and/or via the SNDS-PMSI databases. These data will also be collected for periods before the epidemic to enable comparisons with overall pregnancy outcomes between the two periods. These results can be placed in an international context through collaboration with the European Euro-Peristat network, coordinated by the investigators' research team.
The objective of this multi-regional population-based cohort is to assess the impact of COVID-19 infection during pregnancy on maternal and neonatal health, including rates of perinatal transmission and the influence of diverse management practices on morbidity. The study's focus on this specific population and its population-based coverage complement other facility-based surveillance systems on all cases in France.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- All pregnant or recently pregnant women managed in one maternity unit of the 16 participating perinatal networks
Key inclusion criteria (4 listed)
- Any woman with :
- either proven COVID-19 infection= positive PCR test, OR probable COVID-19 infection = typical clinical symptoms AND typical pulmonary radiology
- during pregnancy or within 42 days postpartum,
- whether or not this diagnosis is followed by hospitalization,
Key exclusion criteria (2 listed)
- Refusal to participate
- Major protected (curator, trusteeship)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| An auto-questionnaire comprising three psychometric scalesthree psychometric scales validated in French: _depression (Edinburgh Postpartum Depression Scale (EPDS)), anxiety (State-Trait Anxiety Inventory (STAI) - and Impact of Event Scale (Revised) (IES-R) | Other | – |
Primary outcome
Joint evaluation of morbi-mortality for mother and child up to 12 weeks postpartum
Time frame: At12 weeks after delivery
Maternal Criterion: Validated Composite Criterion of Severe Maternal Morbidity (Epimoms study ref 7). Neonatal Criterion: Mortality and Composite Criterion of Severe Neonatal Morbidity Perinatal asphyxia (arterial pH to cord-7.15 and/or an excess base - 10mmol/L and/or lactates-6 mmol/L, Apgar score at 5 minutes -7), neonatal encephalopathy, seizures, intraventricular hemorrhage, cerebral infarction, periventricular leucomalacia, ulcerative enterocolite, sepsis, respiratory distress syndrome, bronchopulmonary dysplasia, central catheter, ventilatory support, transfusion
3 secondary outcomes
Number of women infection COVID-19
Time frame: During pregnancy and up to 12 weeks
Severe forms of COVID-19 infection in the mother
Time frame: Until 12 weeks after delivery
Severe neonatal morbidity
Time frame: Until 12 weeks after delivery
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Jul 2026.
- Results publication: PubMed 40396221Diguisto C, Ancel PY, Seco A, Baunot N, Caze C, Crenn-Hebert C, Dupont C, Garabedian C, Lebeaux C, Le Ray C, Letouzey M, Lorthe E, Marrer E, Rouger V, Vayssiere C, Vauloup Fellous C, Bonnet MP, Deneux-Tharaux C. Incidence, Risk Factors and Outcomes of SARS-CoV-2 Infection in Pregnant Women: The COROPREG Population-Based Study. Paediatr Perinat Epidemiol. 2025 Jul;39(5):477-494. doi: 10.1111/ppe.70028. Epub 2025 May 21.
Related trials for covid19 Infection
Not yet recruitingPhase 1
Phase I Open-Label Safety Trial of Pembrolizumab for Neurological Post- Acute Sequelae of SARS-CoV-2 (PD1-PASC I)
Post-Acute COVID-19 Syndrome
Active, not recruitingPhase 1
A Safety and Immunogenicity Trial of OCU500, ChAd36 Vector Encoding SARS-CoV-2 Spike Vaccine Via Intranasal and Inhalational Routes in Previously Vaccinated Adults
COVID-19
Active, not recruiting
Intervention to Address Disparate Mental Health Consequences of COVID-19 Pandemic on Latinx and African Newcomers
Mental Health Issue, Mental Health Disorder
Recruiting
Home-Based Exercise Tele-Rehabilitation After COVID-19
Post SARS-CoV2 (COVID-19)
Not yet recruitingPhase 1
A Safety, Reactogenicity and Immunogenicity Trial of RVX-sCPD9 Booster Intranasal COVID-19 Vaccine
COVID -19
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Pierre Yv Ancel, MD, PhD principal investigator
Assistance Publique - Hôpitaux de Paris
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of covid19 Infection and Pregnancy Complications, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Joint evaluation of morbi-mortality for mother and child up to 12 weeks postpartum (time frame: At12 weeks after delivery). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04463758, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Jul 2026.