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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05881616
Other study ID # IRB-20230193-R
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 18, 2023
Est. completion date May 2026

Study information

Verified date July 2023
Source Zhejiang University
Contact LI Lu, Dr.
Phone 0571-88208596
Email luciali@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study aims to collect serum samples from healthy non-pregnant women, pregnant women with and without Gestational Diabetes Mellitus (GDM). We will analyze the metabolite changes among the three groups using clinical metabolomics and identify potential biomarkers and metabolic pathways. This study will provide scientific evidence for early clinical diagnosis, prevention, control, and treatment research of GDM.


Recruitment information / eligibility

Status Recruiting
Enrollment 480
Est. completion date May 2026
Est. primary completion date May 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - No obvious abnormalities in all inspection items - No history of diabetes - No particular dietary habits - No previous history of other mental illnesses - No history of drug abuse or allergies - No history of smoking or drinking Exclusion Criteria: - Pregnancy complications such as uterine fibroids, hyperthyroidism/hypothyroidism, and antiphospholipid antibody syndrome - Critical illnesses such as cardiovascular disease or abnormal liver/kidney function - Personal history of syphilis, HIV positive, and other infectious diseases - Artificial insemination or IVF pregnancy - Multiple pregnancy (twins or more) - Patients participating in other clinical studies - Other reasons that researchers think are inappropriate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Specimen samples and baseline data collection
The remaining serum samples from routine blood tests of subjects will be collected (without additional blood collection), with a serum sample size of approximately 1 mL per subject. The samples will be pre-processed and stored at ultra-low temperatures. At the same time, clinical baseline data of subjects will be collected from outpatient or inpatient medical records, including but not limited to age, height, weight, blood pressure, and gestational age.
Specimen samples and baseline data collection
The remaining serum samples from routine blood tests of subjects will be collected (without additional blood collection), with a serum sample size of approximately 1 mL per subject. The samples will be pre-processed and stored at ultra-low temperatures. At the same time, clinical baseline data of subjects will be collected from outpatient or inpatient medical records, including but not limited to age, height, weight, blood pressure, and gestational age.
Specimen samples and baseline data collection
The remaining serum samples from routine blood tests of subjects will be collected (without additional blood collection), with a serum sample size of approximately 1 mL per subject. The samples will be pre-processed and stored at ultra-low temperatures. At the same time, clinical baseline data of subjects will be collected from outpatient or inpatient medical records, including but not limited to age, height, weight, blood pressure, and gestational age.

Locations

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

Sponsors (2)

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

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Content of serum metabolomics Based on non-targeted metabolomics technology, the metabolites in serum were comprehensively detected. Differential metabolites were screened using multivariate statistical analysis. Then quantitatively detect the content of these metabolites to find the differential metabolites with predictive ability for GDM. Second trimester (24-28 gestational weeks)
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