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Recruiting NCT05569772

Semaglutide for the Treatment of Glucose Intolerance in Women With Prior Gestational Diabetes

Conditions: Glucose Intolerance After a Recent History of Gestational Diabetes

Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE3
Enrollment: 252
Sponsor: Universitaire Ziekenhuizen KU Leuven

Location: AZORG Aalst

Summary

Gestational diabetes (GDM) is an important contributor to the increasing prevalence of type 2 diabetes (T2DM). Women with glucose intolerance in early postpartum are a particularly high-risk group with about 50% who will develop T2DM within 5 years after the delivery. Moreover, women with a history of GDM progress more rapidly to T2DM compared to women with similarly elevated glucose levels. Early intervention after the index pregnancy is therefore crucial to prevent T2DM. With the SERENA project, the investigators aim to reduce the risk to develop T2DM with the long-acting GLP-1 agonist semaglutide in women with a recent history of GDM and glucose intolerance in early postpartum.

Eligibility Criteria

Eligible participants are women aged ≥18 years, with a history of GDM diagnosed according to the 2013 WHO criteria (at 24-32 weeks gestation or \

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Source: ClinicalTrials.gov (NCT05569772). StuddyBuddy aggregates publicly available trial information.