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The Effect of Pre-Meal Milk on Blood Glucose Management in Patients with Hyperglycaemia in Pregnancy: A Prospective Cohort Study

The Effect of Pre-Meal Milk on Blood Glucose Management in Patients with Hyperglycaemia in Pregnancy: A Prospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121763
Enrollment
Unknown
Registered
2026-04-02
Start date
2025-01-13
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

hyperglycemia in pregnancy

Interventions

Drinking pre meal milk group:None
Not drinking pre meal milk group:None

Sponsors

The Second Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. 18 - 45 years old; 2. Patients diagnosed with hyperglycemia in pregnancy according to the ‘Guideline of diagnosis and treatment of hyperglycemia in pregnancy (2022) ’; 3. Volunteer to participate and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. History of disease: Individuals with autoimmune diseases, tumors, severe infections, severe liver or kidney dysfunction, hematologic disorders, severe cardiovascular or cerebrovascular diseases (such as myocardial infarction, heart failure, stroke, coronary artery bypass surgery, or angina), mental disorders, syphilis, HIV/AIDS, or other serious conditions; 2. Complications at the time of diagnosis: such as severe anemia or intrauterine growth restriction (IUGR), etc; 3. Medications that may interfere with OGTT: If the pregnant woman is taking medications that could interfere with glycemic test results (such as high-dose steroids, immunosuppressants, etc.) during the oral glucose tolerance test (OGTT).

Design outcomes

Primary

MeasureTime frame
oral glucose tolerance test (OGTT);Fasting blood glucose;Incremental Area Under the Curve (iAUC);Coefficient of Variation (CV);Area under the curve (AUC);2-hour postprandial blood glucose;Standard deviation of blood glucose (SDBG);hemoglobin A1c (HbA1c);Glucose management indicator (GMI);Mean blood glucose (MG);Time in range (TIR);TIme below range (TBR);

Secondary

MeasureTime frame
HOMA2-ß;Mean amplitude of glycemic excursions (MAGE);Largest amplitude of glycemic excursions (LAGE);Disposition index (DI);Mean of daily differences (MODD);Adverse neonatal outcomes;HOMA-ß;Continuous overlapping net glycemic action - n (CONGA-n);Maternal adverse outcomes;Time above range (TAR);Fasting C-peptide (FCP);Fasting insulin (FINS);

Countries

China

Contacts

Public ContactFang Wang

The Second Affiliated Hospital of Wenzhou Medical University

198025@wzhealth.com+86 13587413561

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026