Gestational Diabetes Clinical Trials

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Are There Any Clinical Benefits to Screening for Late -Onset Gestational Diabetes Mellitus?

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

This study aims to screen women who have a negative Gestational diabetes mellitus (GDM) result in routine screening tests or who have never had it with the Fasting Blood Glucose Test (FBG) at 32-34 weeks of gestation to diagnose late-onset GDM with routine FBG ≥5.1 mmol/L (92mg/dl) in fasting blood, and to investigate its connection with perinatal and maternal outcomes, hoping to inform about late-stage GDM.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 45
Healthy Volunteers: t
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• Gestational Age: Confirmed singleton pregnancy between 32+0 and 34+6 weeks of gestation based on the last menstrual period (LMP) and/or first-trimester crown-rump length (CRL) ultrasound measurement.

⁃ Follow-up: Intention and willingness to deliver at the study hospital and complete all planned follow-up visits until the end of the postpartum period.

⁃ Informed Consent: Voluntary agreement to participate in the study evidenced by signed written informed consent.

Locations
Other Locations
Turkey
İzmir Katip Çelebi Atatürk Training and Research
RECRUITING
Izmir
Time Frame
Start Date: 2025-03-13
Estimated Completion Date: 2026-11-10
Participants
Target number of participants: 128
Treatments
late-onset gestational diabetes mellitus
In routine screening tests with Fasting Blood Glucose Test (FBG) at 32-34 weeks of gestation, late-onset GDM will be defined by FBG ≥5.1 mmol/L (92mg/dl), which is routinely checked in fasting blood.
control
In routine screening tests with Fasting Blood Glucose Test (FBG) at 32-34 weeks of gestation, control group will be defined by FBG \<5.1 mmol/L (92mg/dl), which is routinely checked in fasting blood.
Related Therapeutic Areas
Sponsors
Leads: Izmir Ataturk Training and Research Hospital

This content was sourced from clinicaltrials.gov