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Search / Trial NCT05917587

Metformin for the Treatment of Microvascular Dysfunction After Gestational Diabetes

Launched by ANNA STANHEWICZ, PHD · Jun 14, 2023

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Gestational Diabetes Postpartum Vascular

ClinConnect Summary

This clinical trial is exploring how a medication called metformin can help improve blood vessel function in women who have experienced gestational diabetes, which is a type of diabetes that can occur during pregnancy. The researchers want to understand the reasons behind the problems with blood vessels in these women and see if metformin could be a useful treatment before any further health issues develop.

To participate in this study, women need to be between 12 weeks and 5 years after having their baby and either have a history of gestational diabetes or have had a healthy pregnancy. However, women who currently have diabetes, are pregnant, smoke, or have certain heart or metabolic conditions cannot join the trial. If eligible, participants will be able to receive treatment and contribute to valuable research that could improve health outcomes for others in the future.

Gender

FEMALE

Eligibility 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

About Anna Stanhewicz, Phd

Dr. Anna Stanhewicz is a distinguished clinical trial sponsor with a robust background in biomedical research and a focus on innovative therapeutic interventions. Her expertise spans across cardiovascular health, metabolic disorders, and translational medicine, enabling her to effectively lead and oversee clinical studies aimed at advancing patient care. With a commitment to rigorous scientific methodology and ethical standards, Dr. Stanhewicz fosters collaborative environments that drive successful trial outcomes. Her leadership not only emphasizes the importance of patient safety and well-being but also aims to contribute valuable insights to the medical community.

Locations

Iowa City, Iowa, United States

Patients applied

0 patients applied

Trial Officials

Anna Stanhewicz, PhD

Principal Investigator

University of Iowa

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported