Oxidative Stress in Microvascular Dysfunction Following Gestational Diabetes (NCT05946785)

🧪 Interventions in This Study

• Acetylcholine (DRUG)
• insulin aspart (DRUG)

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (1 Sites)

• University of Iowa — Iowa City, Iowa

📞 Contact the Study Coordinator

Phone: (319) 467-1732

Email: anna-stanhewicz@uiowa.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

• 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
• Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
• Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Gestational Diabetes

• Preventing Obstetric Complications With Dietary Intervention — Milwaukee, Wisconsin
• Healthy Eating in Women at Risk of Gestational Diabetes — Québec, Quebec
• Role of Adipokines in Glucose Regulation During Pregnancy and in Fetal Development — Sherbrooke, Quebec
• Predicting Dysglycemia in Individuals With Gestational Diabetes Immediately Postpartum Using Continuous Glucose Monitoring — Calgary, Alberta
• Role of NADPH Oxidase in Microvascular Dysfunction Following GDM — Iowa City, Iowa
• Gestational Diabetes and Pharmacotherapy (GAP) — Milwaukee, Wisconsin

Explore by condition: All Gestational Diabetes clinical trials

💡 How to Participate

1. Check the checklist above to see if you may qualify.
2. Contact the study coordinator using the phone/email above.
3. Ask about the visit schedule, what is covered at no cost, and any travel support.
4. Confirm with your own doctor before making a decision.