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Clinical Trials/NCT05160649
NCT05160649
Active, not recruiting
Not Applicable

Effect of Time of COVID 19 Infection on Fetomaternal Outcome, and Immunological Changes During the Disease Course

Fayoum University1 site in 1 country50 target enrollmentOctober 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Fayoum University
Enrollment
50
Locations
1
Primary Endpoint
First, second and third trimester fetomaternal complications.
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

The novel coronavirus called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was discovered for the first time in December 2019 in Wuhan (China) and the disease it causes is called coronavirus disease 2019 (COVID-19). Now, this pandemic is rapidly spreading all over the world.

Pregnant have higher rates of COVID-19, associated with hospitalizations, and severe in-hospital outcomes. Immune responses may have a potential role in the diagnosis, treatment, and prognosis of patients with COVID-19. So we need of identifying biomarkers for disease severity and progression.

Detailed Description

It is important to define whether a novel virus is transmissible from a mother to her infant, vertical infection, and there are three possible mechanisms for vertical infection - intrauterine infection (including transplacental and ascending infections), intrapartum transmission (during delivery), and postpartum infection. These mechanisms have important implications that can influence obstetrical management decisions, best practice delivery options, and neonatal care (3). Aim of work To detect the effect of time of infection by COVID 19 on the fetomaternal outcome including vertical transmission, and the immunological and genetic changes during the disease course. Patients and Methods: * All pregnant women eligible for the study will undergo detailed medical history. * Each patient will have the following data: • Patient name. • Age. • Past medical and surgical history. • Menstrual history and contraceptive history: especially emphasis on Last Menstrual Period to determine the exact gestational age. * Clinical examination of the patients: - General examination of vital data (blood pressure, pulse, temperature, respiratory rate). CBC, PT, PTT, RBS, ALT, AST, serum creatinine), and ultrasound will be done. * Abdominal examination: to detect any abnormality as intrauterine growth restriction, with serial ultrasound estimation.

Registry
clinicaltrials.gov
Start Date
October 10, 2021
End Date
October 2023
Last Updated
3 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

rehab abdelhamid aboshama

lecturer of obstetrics and gynecology Faculty of medicine

Fayoum University

Eligibility Criteria

Inclusion Criteria

  • Pregnant pt with covid 19 infection (at any gestational age) diagnosis of infection based on any one of the following criteria:
  • Positive RT-PCR nasopharyngeal swab is taken (even if the result became available after labor);
  • Positive rapid antigen test performed before labor
  • Chest computed tomography (CT) scan performed before labor showing changes consistent with pneumonitis secondary to SARS-CoV-2 infection;
  • Positive pre-labor immunoglobulin G or immunoglobulin M antibody test; or
  • Clinical diagnosis made before labor (in the absence of negative RT-PCR swab results).

Exclusion Criteria

  • Healthy individuals:
  • Acute or chronic infectious disease,
  • And any medication with known influence on immunological factors.

Outcomes

Primary Outcomes

First, second and third trimester fetomaternal complications.

Time Frame: 3 months

Abdominal examination: to detect any abnormality as intra uterine growth restriction, with serial ultrasound estimation.

fetal distress

Time Frame: 3 months

Intrapartum fetal heart rate (FHR) to detect viability and any abnormalities. Pregnant women diagnosed to have intrapartum fetal distress (Non reassuring or pathological changes according to NICE guidelines 2017)

Secondary Outcomes

  • fetal outcome(3 months)
  • Time of infection and fetal complications(3 months)

Study Sites (1)

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