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RecruitingNCT05946785

Oxidative Stress in Microvascular Dysfunction Following Gestational Diabetes

Role of Oxidative Stress in Microvascular Dysfunction Following Gestational Diabetes

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
28 (estimated)
Sponsor
Anna Stanhewicz, PhD · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this investigation is to examine the role of oxidative stress in aberrant microvascular function in otherwise healthy women with a history of GDM.

Detailed description

Women with a history of gestational diabetes mellitus (GDM) are at a 2-fold greater risk for the development of overt cardiovascular disease (CVD) following the effected pregnancy. While subsequent development of type II diabetes elevates this risk, prior GDM is an independent risk factor for CVD morbidity, particularly within the first decade postpartum. GDM is associated with impaired endothelial function during pregnancy and decrements in macro- and microvascular function persist postpartum, despite the remission of insulin resistance following delivery. Collectively, while the association between GDM and elevated lifetime CVD risk is clear, and available evidence demonstrates a link between GDM and vascular dysfunction in the decade following pregnancy, the mechanisms mediating this persistent dysfunction remain unexamined. The purpose of this investigation is to examine the role of oxidative stress in mediating vascular dysfunction in women who have had gestational diabetes. In this study, the investigators use the blood vessels in the skin as a representative vascular bed for examining mechanisms of microvascular dysfunction in humans. Using a minimally invasive technique (intradermal microdialysis for the local delivery of pharmaceutical agents) they examine the blood vessels in a dime-sized area of the skin in women who have had GDM. As a compliment to these measures, the investigators also collect endothelial cells from an antecubital vein and measure markers of oxidative stress and insulin-mediated eNOS phosphorylation in these cells.

Conditions

Interventions

TypeNameDescription
DRUGAcetylcholineacetylcholine is perfused at 10 ascending concentrations (10\^-10M - 10\^-1 M) for 5 minutes each
DRUGinsulin aspartinsulin aspart is perfused at 5 ascending concentrations (10\^-8M - 10\^-4 M) for 10 minutes each

Timeline

Start date
2023-07-01
Primary completion
2026-12-31
Completion
2027-06-01
First posted
2023-07-14
Last updated
2025-05-13

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05946785. Inclusion in this directory is not an endorsement.