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Exploring the impact of applying CGM-based gestational nutrition management mode on gestational hyperglycemic disorders

Exploring the impact of applying CGM-based gestational nutrition management mode on gestational hyperglycemic disorders

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117783
Enrollment
Unknown
Registered
2026-01-28
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Pregestational Diabetes Mellitus Impaired Fasting Glucose ,Gestational Diabetes Mellitus

Interventions

Experimental Group:Wear Continuous Glucose Monitors and receive online guidance on diet and exercise.

Sponsors

Tongzhou Maternal and Child Health Care Hospital of Beijing
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women who were first diagnosed with gestational hyperglycemia during early to mid-pregnancy and voluntarily participated in the study.According to the "Guidelines for the Diagnosis and Treatment of Hyperglycemia in Pregnancy (2022)," hyperglycemia in pregnancy includes pregestational diabetes mellitus (PGDM), impaired fasting glucose (IFG), and gestational diabetes mellitus (GDM). (1) IFG was diagnosed by fasting blood glucose (FPG) >=5.6mmol/l at the first pregnancy examination. (2) In the first trimester, FPG was in the range of 5.1mmol/1-5.6mmol/1, and fpg>=5.1mmol/l was reexamined at 24-28 weeks to diagnose GDM. OGTT was performed for fpg=5.1mmol/1 or 1h>=10.0mmol/l or 2h>=8.5mmol/l to diagnose GDM. (3) PGDM was diagnosed if the diagnosis was not confirmed before pregnancy and the blood glucose increased during pregnancy reached any of the following criteria: fpg>=7.0mmol/1; Accompanied by typical symptoms of hyperglycemia or hyperglycemic crisis, and any blood glucose >= 11.1mmol/l (except OGTT); Hba1c>=6.5.

Exclusion criteria

Exclusion criteria: 1. Pregnant women with a pre-pregnancy diagnosis of type 1 or type 2 diabetes; 2. Pregnant women with pre-existing underlying conditions, including hypertension, kidney disease, immune system disorders, tumors, impaired glucose tolerance, insulin resistance, coagulation abnormalities, etc; 3. Pregnant women diagnosed during pregnancy with underlying conditions such as kidney disease, immune system disorders, tumors, coagulation abnormalities, etc.

Design outcomes

Primary

MeasureTime frame
Pregnancy Complications;Adverse Pregnancy Outcomes;Adverse Neonatal Outcomes;

Secondary

MeasureTime frame
Acceptability;Blood glucose related indicators;Types and Dosages of Insulin;Medical costs, social costs;

Countries

China

Contacts

Public ContactJiao Yujie

Tongzhou Maternal and Child Health Care Hospital of Beijing

jyjbobo2021@163.com+86 182 1018 9395

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026