IRB Study Number 25-679
Status Recruiting
Location Cleveland Clinic Main Campus
Institute Endocrinology and Metabolism Institute
Description
The purpose of this study is to learn more about blood sugar control in polycystic ovarian syndrome.
Inclusion Criteria
Adult 18-45 years old
Diagnosis of PCOS by usual clinical method such as by Rotterdam criteria
BMI ++>++25 kg/m2
Exclusion Criteria
Currently on medications that can improve glucose levels such as metformin and glucagon-like receptor 1 agonists (GLP1RA)
Previously intake of above-mentioned medications but less than 3 months since last intake of metformin or less than 6 months since last intake of GLP1RA
Currently on insulin
Does not have Stelo-compatible phone
Fasting glucose ++>++100 mg/dL (because that is the cutoff for prediabetes) (either labs taken within a week after first visit or within 3 months before start of study
HbA1c ++>++ 5.7% (because this is the cutoff for prediabetes) (either labs taken after screening visit or within 3 months before start of study)
History of anorexia or bulimia
Current or previous CGM use
Use of oral contraceptives at time of enrolment
Pregnant or with intent to become pregnant within 6 months (will need to terminate study if gets pregnant as glucose readings will be affected)
Menopausal women
Pacemaker or implantable device
Intake of hydroxyurea, or acetaminophen >4 g a day
Allergy to Stelo components including adhesive