Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1000 participants
OBSERVATIONAL
2023-04-01
2026-06-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effects of COVID-19 Infection on Pregnancy Outcomes and Offspring Health
NCT06186947
Clinical Characteristics of Coronavirus Disease 2019 (COVID-19) in Pregnancy
NCT04319016
Maternal and Fetal Outcomes in Pregnant Women With COVID -19,a Cross Sectional Study
NCT05608616
Obstetric and Perinatal Outcomes of Women With COVID-19
NCT04369859
Covid-19 Infection in Pregnancy
NCT04869202
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* Collect the information about Corona Virus Disease 2019 infection and medication of pregnant women to establish a birth cohort, and analyze the correlation between Corona Virus Disease 2019 infection during pregnancy and adverse pregnancy outcomes and birth outcomes.
* The offspring born in this cohort were followed up to analyze the effects of Corona Virus Disease 2019 infection during pregnancy on the nervous system development of the offspring.
Researchers will compare Corona Virus Disease 2019 infection group and uninfected group during pregnancy to see if Corona Virus Disease 2019 infection has adverse effects on pregnant women and their offspring.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Conduct regular physical examinations in the hospital and establish a children's health manual for infants.
* Age ≥ 18 years old
Exclusion Criteria
* Individuals with severe mental disorders.
18 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Qilu Hospital of Shandong University
OTHER
Jinan Maternity and Child Health Care Hospital
UNKNOWN
Shandong Provincial Maternity and Child Health Care Hospital
UNKNOWN
The Second Hospital of Shandong University
OTHER
Qianfoshan Hospital
OTHER
Shandong University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yinuo Song
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Fanzhen Hong, Doctorate
Role: STUDY_DIRECTOR
The Second Hospital of Shandong University
Xia Luo, Doctorate
Role: STUDY_DIRECTOR
Qilu Hospital of Shandong University
Yueqin Xu, Doctorate
Role: STUDY_DIRECTOR
Qianfoshan Hospital
Qiuhong Yang, Doctorate
Role: STUDY_DIRECTOR
Jinan Maternity and Child Health Care Hospital
Jie Chen, Doctorate
Role: STUDY_CHAIR
Shandong University
Yinuo Song, Master
Role: PRINCIPAL_INVESTIGATOR
Shandong University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The Second Hospital of Shandong University
Jinan, Shandong, China
Jinan Maternity and Child Health Care Hospital
Jinan, , China
Qianfoshan Hospital
Jinan, , China
Qilu Hospital of Shandong University
Jinan, , China
Shandong Provincial Maternity and Child Health Care Hospital
Jinan, , China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
LL202303018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.