University of Colorado Anschutz/Children's Hospital Colorado Aurora
Aurora, Colorado, 80045, United States
Location status: Recruiting
NCT Number: NCT05819853
Girls and women 12-35 years old with obesity and polycystic ovarian syndrome who are on or off metformin, will receive a glucagon like peptide-1 receptor agonist intervention for 10 months to induce metabolic changes, weight loss and improve reproductive abnormalities.
Interested in participating?
Request Info12 year–35 year
Female
Interventional
Phase 3
Aurora, Colorado, 80045, United States
Location status: Recruiting
Polycystic ovary syndrome is one of the most common endocrinopathies in women, presents with anovulation in adolescence, and reproductive dysfunction is related to excess weight. After a 4-month observation period of either no medication or metformin treatment, females aged 12-35 years with obesity and polycystic ovary syndrome will receive 10 months of a glucagon-like peptide-1 receptor agonist to induce metabolic changes, weight loss and improve reproductive abnormalities. We will assess the relationship between weight loss and reproductive function, as well as identify if age, hormonal and metabolic measures and such insulin sensitivity and insulin secretion predict the response to glucagon-like peptide-1 receptor agonist therapy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
10 months of semaglutide, with dose escalation as recommended by manufacturer. Maximum dose used will be 1.7mg
Other names: Semaglutide (Wegovy and/or Ozempic)
Time frame: 14 months
The change in ovulation will be measured at baseline and 6-10 months post treatment with semaglutide from 4 months daily urinary progesterone metabolites
Time frame: Baseline and 10 months
Participants will undergo a 75 gram oral glucose tolerance test, and whole body insulin sensitivity will be expressed as Si, calculated via the oral minimal model using SAMM II software. This software uses participant weight, glucose and insulin concentrations at various time points during the oral glucose tolerance test to calculate the participant's insulin sensitivity. A positive Si value means an improvement in insulin sensitivity.
Time frame: Baseline and 10 months
Participants will have an ovarian ultrasound performed to measure change in ovarian morphology: ovarian size and number of follicles pre/post treatment with semaglutide
Contact information is provided by the study sponsor or research team.
University of Colorado, Denver
Other
Acronym: RESTORE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07182526
Adnexal Diseases, Cysts
Baghdad, Karkh, Iraq
View Trial DetailsNCT06041204
Adnexal Diseases, Cysts
Cairo, Egypt
View Trial DetailsNCT05734287
Adnexal Diseases, Cysts
Doha, Qatar
View Trial DetailsNCT05756023
Adnexal Diseases, Cysts
Asyut, Egypt
View Trial Details