Covid19 Clinical Trial
Official title:
Impact of COVID-19 Infection on the Course of Pregnancy and Fetal-neonatal Outcomes
NCT number | NCT04699578 |
Other study ID # | 8453 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | December 28, 2020 |
Est. completion date | May 1, 2022 |
COVID-19, the coronavirus responsible for the pandemic that began at the end of 2019 in China, spreads through respiratory droplets and direct contact. The most common symptoms of the disease include fever, cough, asthenia or myalgia, wheezing and headache, and the most serious complication is acute respiratory distress syndrome (ARDS). The new coronavirus has continued to spread to multiple countries and continents so much so that the epidemic was declared a Public Health Emergency of International Interest (PHEIC) by the World Health Organization (WHO) on January 30, 2020. In the first phase of emergency worldwide, characterized by high morbidity and mortality, scientific interest has been mainly directed to the study of the transmission mechanisms of the infection, diagnostic tools and therapies for ARDS, especially in elderly and co-morbid patients. Interest has rapidly spread to other categories of patients and in particular to pregnancy, on which the virus could impact in different ways, with consequences for both the mother and the fetus. A recent systematic review that included all published reports on Coronaviruses (COVID-19, SARS, and MERS) in pregnancy showed that preterm delivery is the most frequently reported adverse event in these women, and that COVID-19 is associated with an increased risk of preeclampsia and caesarean section. Nonetheless, the limited sample size, the main inclusion of cases reported for acute respiratory symptoms, the lack of information on previous pathologies potentially capable of complicating pregnancy, do not allow for the extrapolation of strong evidence on the course of infection in pregnancy. Therefore, the current status of the scientific literature does not allow for general and wide-ranging implications. THe investigators therefore believe it is particularly useful to investigate maternal and fetal outcomes in this new broader scenario, including all pregnancies associated with asymptomatic or symptomatic SARS-CoV-2 infection, found in any gestational period, in order to evaluate in a "real world scenario" "Actual rates of maternal-fetal and neonatal adverse events
Status | Recruiting |
Enrollment | 230 |
Est. completion date | May 1, 2022 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Maternal age> 18 years - Women with single or multiple pregnancy at any stage of gestation, with first ascertained positivity to the nasopharyngeal swab for SARS-CoV-2 during pregnancy, regardless of the presence of symptoms. Exclusion Criteria: - age under 18. - Women with an altered state of consciousness, seriously ill, with mental handicaps; - Women with serious systemic diseases that can negatively affect the pregnancy outcome. - Women for whom the treating doctor contraindicates participation in the study. |
Country | Name | City | State |
---|---|---|---|
Italy | University of Campania Luigi Vanvitelli | Naples |
Lead Sponsor | Collaborator |
---|---|
University of Campania "Luigi Vanvitelli" |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Preterm birth rate | Less than 37 weeks gestation | ||
Secondary | Gestational age at delivery | Time of delivery | ||
Secondary | Preterm birth rates | Less than 24, 28, 34 weeks gestation | ||
Secondary | Birth weight | Weight of the baby at the time of delivery | Time of delivery | |
Secondary | Composite adverse neonatal outcomes | Number of neonates who will have at least one of the following:
necrotizing enterocolitis (NEC), intraventricular hemorrhage (IVH) (grade 3 or higher), respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), retinopathy (ROP), blood-culture proven sepsis and neonatal death |
Between birth and 28 days of age | |
Secondary | Maternal outcomes | Number of mothers who will have at least one of the following:
sepsis, histological chorioamnionitis, hysterectomy, intensive care unit admission. |
Between birth and 28 days after the birth | |
Secondary | Inflammatory markers: coagulation profile, C-reactive protein, glycaemia, ferritinemia | Through study completion, an average of 6 months |
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