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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04744714
Other study ID # GWG2021
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2021
Est. completion date December 31, 2024

Study information

Verified date February 2023
Source Women's Hospital School Of Medicine Zhejiang University
Contact Zhaoxia Liang, M.D.
Phone 86571-87061501
Email xiaozaizai@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Appropriate gestational weight gain (GWG) is a key factor in balancing maternal and neonatal needs of nourishment and health, which is especially important in women with gestational diabetes mellitus (GDM). However, there are no specific guidelines for GWG in Chinese pregnant women and even for GDM pregnant women.This project intends to fill in the gaps of this field through multi-center large sample prospective cohort study.


Description:

Inappropriate gestational weight gain (GWG) is an important risk factor affecting adverse pregnancy outcomes. However, the current guidelines for GWG are based on American population and may not apply to pregnant women in China, especially for those with gestational diabetes mellitus (GDM) who have high risk factors. The big gaps in academic-related fields need to be filled. Our research group has previously found the heterogeneous relationships between GWG and adverse outcomes in GDM women with different abnormal glucose metabolism. Therefore, based on the principles of precision medicine, this project intends to establish for the first time the GWG standard for Chinese pregnant women to optimize the GWG management through a multicenter prospective cohort study. At the same time, specific GWG guidelines applicable to GDM women with different glucose metabolism abnormalities were innovatively constructed. Our study will provide strong evidence for stratified management and precise intervention of GDM pregnant women, which is of great significance to ensure health of both mothers and their offspring.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 49 Years
Eligibility Inclusion Criteria: - Maternal age: 20-49 years; - Natural conception; - Single pregnancy; - Plan to have routine prenatal examinations and give birth in the research center; - No plan to move within two years; - No second pregnancy within two years; - Willing to cooperate with the hospital to follow up after childbirth. Exclusion Criteria: - Have diseases that affect metabolic function or even threaten the life of the mother and fetus before pregnancy, such as diabetes, hypertension, heart disease, liver and kidney diseases, thyroid diseases, autoimmune diseases, malignant tumors, AIDS, etc.; - Assisted reproduction; - Multiple pregnancy; - Fetus has a known deformity or genetic defects; - Incomplete clinical data.

Study Design


Locations

Country Name City State
China Women's Hospital School of Medicine Zhejiang University Hangzhou

Sponsors (1)

Lead Sponsor Collaborator
Women's Hospital School Of Medicine Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maternal outcomes Including pregnancy-induced hypertension, preterm delivery, abortion, delivery way and so on. They are diagnosed by clinicians and the data is gathered from medical records. Through delivery completion, up to 40 weeks
Primary Neonatal outcomes Birth weight(in gram), birth height (in centimetre), gestational week (in week) and so on. They are diagnosed by clinicians and the data is gathered from medical records. Through delivery completion, up to 40 weeks
Secondary glucose metabolism index OGTT results (mmol/L), HbA1c (%) and so on postpartum 42 days
Secondary offspring weight (in gram), height (in centimetre), feeding situation (breast feeding or artificial feeding) and so on. postpartum 42 days
Secondary annual follow-up results Annual questionnaire and physical examination, including weight (in kilogram), height (in metre), disease history, diet surveys and so on. 1 or 2 years after delivery
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