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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05125770
Other study ID # KY2021-12
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 8, 2021
Est. completion date December 30, 2024

Study information

Verified date November 2021
Source Beijing Ditan Hospital
Contact Wei Yi, Doctor
Phone 13683687062
Email yiwei1215@163.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

All the pregnant women and newborns of both or one of the couples who gave birth in Ditan hospital were collected as the observation group, and the pregnant women and newborns of both husband and wife who gave birth in our hospital without new crown vaccine during pregnancy were collected as the control group. The incidence of adverse events during pregnancy of the two groups and the incidence of intrauterine development and congenital malformations of the two groups were observed to observe the physical and intellectual development of children in the two groups at the age of 1 year, and to explore the safety of perinatal neocrown vaccination.


Description:

This study is a prospective observational cohort study. All the pregnant women and newborns of both or one of the couples who gave birth in Ditan hospital were collected as the observation group, and the pregnant women and newborns of both husband and wife who gave birth in our hospital without new crown vaccine during pregnancy were collected as the control group. The incidence of adverse events during pregnancy of the two groups and the incidence of intrauterine development and congenital malformations of the two groups were observed to observe the physical and intellectual development of children in the two groups at the age of 1 year, and to explore the safety of perinatal neocrown vaccination.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 30, 2024
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - The pregnant women and newborns who were injected with the new crown vaccine during the perinatal period of both husband and wife or one of them were the observation group, and the pregnant women and newborns who were not vaccinated with the new crown vaccine during the perinatal period of both husband and wife were the control group. They were fully informed of the risk, voluntarily joined the study and signed the informed consent. Exclusion Criteria: - Both husband and wife or family have previously delivered congenital abnormal fetus; - Neither husband nor wife was willing to participate in this study.

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
New crown vaccine
New Coronavirus vaccine

Locations

Country Name City State
China Beijing Ditan Hospital, Capital Medical University Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Ditan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Neonatal congenital malformation rate Observe whether the newborn has malformation at birth
Primary Intellectual development of 1-year-old children The intellectual development of newborns was observed at one year old
Secondary Incidence of maternal adverse events during pregnancy Observe the incidence of maternal adverse events during pregnancy during pregnancy
Secondary Physical development of children at birth and 1 year old Observe the physical development of children at birth and 1 year old at birth, at 1 year old
Secondary The incidence of adverse events among children aged 1 year Observe the incidence of adverse events among children aged 1 year among 1 year old
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