Understanding Microvascular Dysfunction After Gestational Diabetes
This study is looking into why women who have had gestational diabetes (diabetes during pregnancy) might have problems with their small blood vessels (microvascular dysfunction) later on. Researchers will use a minimally invasive technique on a small area of skin to see how your blood vessels react to two different substances: acetylcholine and insulin aspart. They want to understand if oxidative stress (an imbalance in the body that can damage cells) plays a role. The main goal is to measure how well your small blood vessels widen in response to acetylcholine and insulin aspart. This study plans to include 28 women, aged 18-50, who have either had gestational diabetes within the last five years or have no history of it. The study is currently unclear on its recruitment status.
- Study design
- This is an interventional study planning to enroll 28 women. It is not specified if it is randomized or blinded.
- What's involved
- You would participate in a single study visit lasting about 4 hours, during which substances will be applied to a small area of your skin.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your microvascular dilation will be measured at the study visit, which lasts about 4 hours. No further follow-up is specified.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Oxidative Stress in Microvascular Dysfunction Following Gestational Diabetes
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- microvascular acetylcholine-mediated dilationat the study visit, an average of 4 hours
cutaneous vascular vasodilator responses to acetylcholine perfusion in lactated Ringer's, ascorbate, and L-NAME treated microdialysis sites
- microvascular insulin-mediated dilationat the study visit, an average of 4 hours
cutaneous vascular vasodilator responses to insulin perfusion in lactated Ringer's, ascorbate, and L-NAME treated microdialysis sites