Metformin for the Treatment of Microvascular Dysfunction After Gestational Diabetes
Anna Stanhewicz, PhD · NCT05917587
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–45 · Women only
- Healthy volunteers
- Accepted
- Study type
- Interventional · Early Phase 1
- Target enrollment
- 30
- US sites recruiting
- 1
- Study start
- September 11, 2024
- Record last updated
- May 13, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this investigation is to examine the mechanisms mediating vascular dysfunction in women who have had gestational diabetes and how metformin may be a valuable treatment tool to improve microvascular function in these women before the onset of disease.
Being studied: Metformin Hydrochloride; placebo
Conditions: Gestational Diabetes
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- ≥12 weeks and ≤5 years postpartum
- history of GDM or healthy pregnancy
Exclusion Criteria
- prediabetes or diabetes (HbA1c ≥5.7%)
- current tobacco use
- cardiovascular or metabolic disease
- cardiovascular or metabolic medication
- history of hypertension during pregnancy
- current pregnancy
Recruiting US locations
University of Iowa
Iowa City, IA 52242
Site contact: Anna Stanhewicz, PhD · 319-467-1732 · anna-stanhewicz@uiowa.edu
Study contacts (from the official record)
- Anna Stanhewicz, PhD · 3194671732 · anna-stanhewicz@uiowa.edu
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