Clinical Trials Directory

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UnknownNCT05160649

Effect of Covid 19 Infection on Fetomaternal Outcome

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

Status
Unknown
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Fayoum University · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2021-10-10
Primary completion
2023-06-01
Completion
2023-10-01
First posted
2021-12-16
Last updated
2023-04-28

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05160649. Inclusion in this directory is not an endorsement.