Pregnancy Outcomes According to the Gestational Age of Acquiring COVID-19

September 1, 2021 updated by: Jani Jacques, Brugmann University Hospital

Pregnancy Outcomes According to the Gestational Age of Acquiring COVID-19 : an International Case-control Study

A new coronavirus, called severe acute respiratory syndrome coronavirus 2 (SARS-CoV2) appeared in Wuhan, China and it arrived to Europe 2-3 months later. It infected millions of persons and led to the death of thousands until May 2020 where numbers of infections per week decreased significantly. However, starting September, number of infections started to escalate again and continued to rise until now.

Hundreds of good quality articles were published during this period to study the relationship and effects of this virus on pregnancy and vice versa, as well as to determine the adverse neonatal and obstetrical outcomes following the infection. In a case-control study using propensity score matching at the level of age, body mass index and comorbidities (diabetes, hypertension, asthma), pregnant women over 20 week's gestation had significantly higher risk for intensive care unit stay, endotracheal intubation, hospitalization for disease related symptoms and need for oxygen therapy. A new systematic review also demonstrated increased risk for ICU admission in pregnant women compared to non-pregnant women and to non-infected pregnant women.

On the other hand, many researchers have demonstrated that the rates of preterm delivery and cesarean delivery have increased as well, others reported a close relation between SARS-CoV2 infection and preeclampsia or preeclampsia like condition. Enormous effort was done in order to understand adverse outcomes related to this infection, however, most studies included patients in the third or late second trimester. Few studies stratified adverse outcomes of the patients according to the trimester of infection.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

10925

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Brussels, Belgium, 1020
        • CHU Brugmann
      • Clamart, France, 92140
        • Antoine Béclère Hospital
      • Colombes, France, 92700
        • Hopital Louis Mourier
      • Roma, Italy, 00168
        • Fondazione Policlinico Universitario Agostino Gemelli

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Study population will include all pregnant women with viable fetus after 10 weeks' gestation and known pregnancy outcome during the period starting on February 1st 2020 and ending on November 30th 2020.

Description

Inclusion Criteria:

Pregnant women with viable fetus after 10 weeks' gestation and known pregnancy outcome during the period starting on February 1st 2020 and ending on November 30th 2020.

Exclusion Criteria:

All ongoing pregnancies, those with unknown outcomes, those terminated medically or voluntary, as well as patients with spontaneous abortion before the 11th gestational week.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
COVID positive <20 weeks
Case groups 1 will include pregnant patients infected by SARS-CoV2 before 20 weeks' gestation during the period starting on February 1st 2020 and ending on November 30th 2020.
Data extraction from medical files
COVID positive >20 weeks
Case groups 2 will include pregnant patients infected by SARS-CoV2 after 20 weeks' gestation during the period starting on February 1st 2020 and ending on November 30th 2020.
Data extraction from medical files
Control
Patients not infected by SARS-CoV2 during pregnancy during the period starting on February 1st 2020 and ending on November 30th 2020
Data extraction from medical files

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Preterm delivery
Time Frame: 5 minutes
Delivery at a gestational age < 37 weeks
5 minutes
Preeclampsia
Time Frame: 5 minutes

Preeclampsia is defined as elevated blood pressure (Systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg on at least 2 occasions at least 4 hours apart after 20 weeks of gestation in a previously normotensive patient) and the new onset of 1 or more of the following:

  • Proteinuria ≥0.3 g in a 24-hour urine specimen or protein/creatinine ratio ≥0.3 (mg/mg) (30 mg/mmol) in a random urine specimen or dipstick ≥2+ if a quantitative measurement is unavailable
  • Platelet count <100,000/microL
  • Serum creatinine >1.1 mg/dL (97.2 micromol/L) or doubling of the creatinine concentration in the absence of other renal disease
  • Liver transaminases at least twice the upper limit of the normal concentrations for the local laboratory
  • Pulmonary edema
  • New-onset and persistent headache not accounted for by alternative diagnoses and not responding to usual doses of analgesics
  • Visual symptoms (eg, blurred vision, flashing lights or sparks, scotomata)
5 minutes
Eclampsia
Time Frame: 5 minutes
Eclampsia is defined by the occurrence of a grand mal seizure in a woman with preeclampsia in the absence of other neurologic conditions that could cause seizure.
5 minutes
Hemolysis Elevated Liver enzymes Low Platelets Syndrome (HELLP)
Time Frame: 5 minutes
HELLP syndrome is considered to be a serious complication or variant of preeclampsia in pregnant women.
5 minutes
Number of participants with Cesarean delivery (CD)
Time Frame: 5 minutes
Number of participants with Cesarean delivery (CD)
5 minutes
Percentage of participants with Cesarean delivery (CD)
Time Frame: 5 minutes
Percentage of participants with Cesarean delivery (CD)
5 minutes
Deep venous thrombosis
Time Frame: 5 minutes
diagnosed by imaging tools such as venous Doppler ultrasound of the lower limbs
5 minutes
Pulmonary embolism
Time Frame: 5 minutes
diagnosed by imaging tools such as angio-CT scan of the thorax.
5 minutes
Pregnancy loss at less than 24 weeks' gestation
Time Frame: 5 minutes
5 minutes
Intrauterine Fetal Demise (IUFD)
Time Frame: 5 minutes
Pregnancy loss at 24 weeks or more, or the delivery of a neonate weighing more than 500 g
5 minutes
Maternal death
Time Frame: 5 minutes
Maternal death
5 minutes
Low birth weight
Time Frame: 5 minutes
birth weight at less than 2500g
5 minutes
Number of participants with Neonatal intensive care unit (NICU) admission
Time Frame: 5 minutes
Number of participants with Neonatal intensive care unit (NICU) admission
5 minutes
Percentage of participants with Neonatal intensive care unit (NICU) admission
Time Frame: 5 minutes
Percentage of participants with Neonatal intensive care unit (NICU) admission
5 minutes
Number of participants with APGAR score (Activity, Pulse, Grimace, Appearance, Respiration score) at 5 minutes < 7:
Time Frame: 5 minutes
The score minimum is 0 and maximum is 10. Higher score means better outcome.
5 minutes
Percentage of participants with APGAR score (Activity, Pulse, Grimace, Appearance, Respiration score) at 5 minutes < 7:
Time Frame: 5 minutes
The score minimum is 0 and maximum is 10. Higher score means better outcome.
5 minutes
Number of participants with Respiratory distress at birth
Time Frame: 5 minutes
Number of participants with Respiratory distress at birth
5 minutes
Percentage of participants with Respiratory distress at birth
Time Frame: 5 minutes
Percentage of participants with Respiratory distress at birth
5 minutes
Neonatal death
Time Frame: 5 minutes
5 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants with Delivery < 32 weeks
Time Frame: 5 minutes
5 minutes
Percentage of participants with Delivery < 32 weeks
Time Frame: 5 minutes
5 minutes
Number of participants with Spontaneous delivery < 37 weeks
Time Frame: 5 minutes
5 minutes
Percentage of participants with Spontaneous delivery < 37 weeks
Time Frame: 5 minutes
5 minutes
Number of participants with Fetal distress
Time Frame: 5 minutes
referred to bradycardia, recurrent late or variable deceleration on antepartum or intrapartum cardiotocogram.
5 minutes
Percentage of participants with Fetal distress
Time Frame: 5 minutes
referred to bradycardia, recurrent late or variable deceleration on antepartum or intrapartum cardiotocogram.
5 minutes
Number of participants with Unscheduled cesarean delivery
Time Frame: 5 minutes
5 minutes
Percentage of participants with Unscheduled cesarean delivery
Time Frame: 5 minutes
5 minutes
Postpartum hemorrhage
Time Frame: 5 minutes
defined as the estimated blood loss of > 500 mL
5 minutes
Number of participants with Intraventricular hemorrhage
Time Frame: 5 minutes
5 minutes
Percentage of participants with Intraventricular hemorrhage
Time Frame: 5 minutes
5 minutes
Umbilical cord pH
Time Frame: 5 minutes
5 minutes
Small for gestational age (SGA)
Time Frame: 5 minutes
it refers to an estimated fetal weight of less than the 10th percentile
5 minutes
Large for gestational age (LGA)
Time Frame: 5 minutes
it refers to an estimated fetal weight of more than the 95th percentile
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jacques Jani, MD, CHU Brugmann

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 8, 2020

Primary Completion (Actual)

September 1, 2021

Study Completion (Actual)

September 1, 2021

Study Registration Dates

First Submitted

March 1, 2021

First Submitted That Met QC Criteria

March 1, 2021

First Posted (Actual)

March 3, 2021

Study Record Updates

Last Update Posted (Actual)

September 2, 2021

Last Update Submitted That Met QC Criteria

September 1, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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