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NCT07483723Recruiting

Glucose Profiles in Women With Polycystic Ovary Syndrome

Source: ClinicalTrials.gov · Last updated 19 Mar 2026

Brief summary (registry, in English)

Polycystic ovary syndrome is a very common condition that is associated with metabolic complications. Patients with polycystic ovary syndrome exhibit insulin resistance and are at greater risk to develop type 2 diabetes. This syndrome is heterogeneous, classified according to 4 phenotypes (A-D). It seems that certain phenotypes are less exposed to insulin resistance and metabolic complications. However, only a few studies have evaluated the glucose profile according to phenotype. New technologies now make it possible to monitor glucose levels continuously. The aim of this project is to evaluate glucose profile parameters using continuous glucose monitoring, and to compare these profiles according to different PCOS phenotypes.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
6 Mar 2026
Start date
6 Jan 2026
Primary completion date
Jul 2027
Lead sponsor
Centre Hospitalier Universitaire, Amiens
NCT number
NCT07483723

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 6 Jan 2026 to the primary completion date, Jul 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient treated within 3 months prior to inclusion/data collection with estrogen-progestin contraception, progestin contraception, antidiabetic drugs, inositol, antiandrogen

Other illness

  • Differential diagnoses: hyperprolactinemia, dysthyroidism, Cushing's syndrome, congenital adrenal hyperplasia, virilizing tumor (ovarian or adrenal), intake of exogenous androgens
  • Pre-existing diabetes

Other

  • Pregnancy, breast-feeding

Who the study is looking for

  • Age \> 18 years at inclusion criteria
  • Patient with polycystic ovary syndrome, defined by the presence of at least 2/3 irregular menstrual cycles, clinical or biological hyperandrogenism, polycystic ovary morphology (pelvic ultrasound) or elevated AMH levels, after the exclusion of other disorders.
  • Agreed to carry the FSL pro
  • Signed informed consent

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHRU Amiens
Coordinator of this site? Confirm its status
SalouëlFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.