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NCT04257500CompletedPhase 4

Does Vaginal Delivery of Combined Hormonal Contraception Affect the Risk of Metabolic Syndrome in Overweight/Obese Women With PCOS

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

A prospective study to determine the metabolic effects of the contraceptive vaginal ring among overweight and obese women with polycystic ovary syndrome (PCOS). We will recruit a total of 40 participants and study use of the vaginal ring over a 4-month period.

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
22 (actual)
First submitted
31 Jan 2020
Start date
3 Sept 2020
Primary completion date
22 Aug 2025
Lead sponsor
Andrea Roe, MD, MPH
Diseases
Obesity
NCT number
NCT04257500

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 22
  • From 3 Sept 2020 to the primary completion date, 22 Aug 2025
  • 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

  • Second-trimester pregnancy within four weeks prior to initiation of NuvaRing or third-trimester pregnancy within 6 months prior to initiation of NuvaRing
  • Use of hormonal contraception within four weeks prior to initiation of NuvaRing

Lab values

  • Diagnosis of metabolic syndrome. Metabolic syndrome will be defined according to the updated Adult Treatment Panel III as 3 or more of the following criteria: blood pressure ≥130/85 mm Hg, waist circumference \>35 inches, fasting glucose ≥110 mg/dL, TG ≥150 mg/dL, HDL-C \<50 mg/dL.
  • Medical comorbidities:
    • 21-hydroxylase deficiency, congenital adrenal hyperplasia
    • Untreated thyroid disease
    • Untreated hyperprolactinemia
    • Type 1 or 2 diabetes mellitus
    • Uncontrolled liver disease
    • Uncontrolled renal disease
    • Current alcohol abuse
    • Hypertension ≥ 140 mm Hg average systolic or ≥ 90 mm Hg average diastolic in women using anti-hypertensive medication
    • Hypertension ≥ 150 mm Hg average systolic or ≥ 100 mm Hg average diastolic in women not using anti-hypertensive medication
    • History of or current gynecologic cancer
    • Triglycerides \>=250 mg/dL
    • Current use of lipid-lowering or weight loss agents
    • Participation in any study of an investigational drug or device or biologic agent within 30 days
    • Suspected adrenal or ovarian tumor secreting androgens
    • Suspected Cushing's syndrome
    • Bariatric surgery within 12 months
    • Other medical concerns that in the judgment of the investigator may compromise safety of the participant or confound the reliability of compliance and information acquired in this study

Age

  • Contraindications to NuvaRing use:
    • Age ≥ 35 plus tobacco use
    • Current or past deep vein thrombosis or pulmonary embolism
    • Cerebrovascular disease
    • Coronary artery disease
    • Thrombogenic valvular or rhythm diseases of the heart (such as subacute bacterial endocarditis with valvular disease or atrial fibrillation)
    • Inherited or acquired coagulopathy
    • Headaches with focal neurological symptoms or migraine headaches with aura
    • Age ≥ 35 plus any migraine headaches
    • Liver tumors, benign or malignant
    • Undiagnosed abnormal uterine bleeding
    • Current or past breast cancer or other estrogen- or progestin-sensitive cancer
    • Hypersensitivity to any of the components of NuvaRing
    • Use of hepatitis C drug combinations containing ombitasvir/paritaprevir/ritonavir

Other

  • Current pregnancy or desire for pregnancy during course of study
  • Current breastfeeding

Who the study is looking for

  • Diagnosis of PCOS according to Rotterdam criteria, with at least 2 of 3 of the following criteria: oligomenorrhea (≤8 periods per year), clinical or biochemical hyperandrogenism, and polycystic ovaries on ultrasound
  • Body mass index ≥25 and ≤45 kg/m2
  • In good general health according to the investigators' discretion
  • Willing to avoid pregnancy for the duration of the study

Age in the registry: 18 years to 40 years · 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
University of Pennsylvania
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status

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