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A Risk Score for Prediction of Gestational Diabetesmellitus in China Using Routinely Collected Hospital Data

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Completed

Conditions

Gestational Diabetes Mellitus (GDM)

Treatments

Other: Collect clinical data of pregnant women

Study type

Observational

Funder types

Other

Identifiers

NCT07160920
JS-2763

Details and patient eligibility

About

This project will recruit 6,608 pregnant women in the early stage of pregnancy in Beijing and across the country. Researchers (prenatal examination doctors) will collect the basic information of pregnant women and the results of early pregnancy laboratory tests through hospital systems (HIS and LIS systems). The dietary frequency and exercise information of pregnant women were collected through questionnaire surveys: A 75g oral glucose tolerance test (0GTT test) was conducted at 24-28 weeks. Follow-up was conducted until the completion of the 75gOGTT test, and the delivery outcomes were recorded. By making the subjects pay attention to their own physical conditions through the project, abnormalities can be detected early. At the same time, early prediction of gestational diabetes mellitus enables doctors and health physicians to identify high-risk groups for gestational diabetes mellitus (GDM) at an early stage and carry out early intervention, reducing GDM and related pregnancy complications, promoting the health of mothers and infants, and reducing the additional medical expenses that may be borne for GDM management and the overall medical expenditure of the country in the future.

Enrollment

6,608 patients

Sex

Female

Ages

21 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All pregnant women with single pregnancies in the early stage of pregnancy who have registered in the hospital are eligible to participate in the proposed program.

Exclusion criteria

Pregnant women with a known history of type 1 or type 2 diabetes will be excluded.

Trial design

6,608 participants in 1 patient group

pregnant woman
Treatment:
Other: Collect clinical data of pregnant women

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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