Early Diagnosis of GDM by Multiomics

Sponsor
Women's Hospital School Of Medicine Zhejiang University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05386927
Collaborator
(none)
400
1
32
12.5

Study Details

Study Description

Brief Summary

Gestational diabetes mellitus (GDM) is prone to cause a variety of adverse pregnancy outcomes, and has potential harm to the short-term and long-term health of both mothers and infants. However, its diagnosis mainly relies on oral glucose tolerance test (OGTT) at 24-28 weeks of gestation, so it is often diagnosed in the second and third trimester, and may be too late to intervene. Therefore, advancing the diagnostic window period of GDM is the key to the prevention and treatment of GDM and its complications. It is urgent to establish a new technology for the early diagnosis and screening of GDM with high detection rate and accuracy. Based on literature survey and previous studies, this study found that the combined analysis of metabolomics and lipidomics may have broad clinical application prospects in the early diagnosis and screening of GDM. It is hoped that a set of new techniques based on multi-omics for early diagnosis and screening of GDM can be constructed, providing a feasible and effective tool for early detection and treatment of GDM in clinical.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire survey and specimen collection

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Clinical Study of a New Technology System for Early Diagnosis and Screening of GDM Based on Multiomics
Actual Study Start Date :
May 1, 2022
Anticipated Primary Completion Date :
May 1, 2023
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
GDM group

Pregnant women with positive OGTT results at 24-28 gestational weeks

Other: Questionnaire survey and specimen collection
A questionnaire survey was conducted when pregnant women were enrolled in the first trimester, and blood, urine, saliva and other specimens were collected.

Control group

Pregnant women with negative OGTT results at 24-28 gestational weeks, and had baseline data that matched those in the GDM group

Other: Questionnaire survey and specimen collection
A questionnaire survey was conducted when pregnant women were enrolled in the first trimester, and blood, urine, saliva and other specimens were collected.

Outcome Measures

Primary Outcome Measures

  1. Salivary metabolomics [First trimester (9-14 gestational weeks)]

    The differential salivary metabolism molecules in saliva were detected by the self-developed detection chip, and the markers related to GDM in early pregnancy were screened. Specimens were collected during the first trimester.

  2. Serum lipidomics [First trimester (9-14 gestational weeks)]

    The differential serum lipid molecules in serum were detected by the self-developed detection chip, and the markers related to GDM in early pregnancy were screened. Specimens were collected during the first trimester.

  3. Urine metabolomics [First trimester (9-14 gestational weeks)]

    The differential urine metabolism molecules in urine were detected by the self-developed detection chip, and the markers related to GDM in early pregnancy were screened. Specimens were collected during the first trimester.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 49 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Plan to have routine prenatal examinations and give birth in the research center

  • First trimester

  • Singleton pregnancy

  • Without pregnancy complications

  • Willing to cooperate with the hospital to follow up

Exclusion Criteria:
  • Have diseases that affect metabolic function or even threaten the life of the mother and fetus before pregnancy, such as diabetes, heart disease, liver and kidney diseases, thyroid diseases with drug, autoimmune diseases, malignant tumors, AIDS, etc.

  • Fetus has a known deformity or genetic defects

  • Incomplete clinical data

Contacts and Locations

Locations

Site City State Country Postal Code
1 Women's Hospital School Of Medicine Zhejiang University Hangzhou Zhejiang China 310006

Sponsors and Collaborators

  • Women's Hospital School Of Medicine Zhejiang University

Investigators

  • Study Director: Zhaoxia Liang, Prof., Women's Hospital School Of Medicine Zhejiang University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Women's Hospital School Of Medicine Zhejiang University
ClinicalTrials.gov Identifier:
NCT05386927
Other Study ID Numbers:
  • IRB-20210293-R
First Posted:
May 23, 2022
Last Update Posted:
May 23, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 23, 2022