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Completed

NCT Number: NCT03981861

Metabolic and Neuro-Endocrine Effect of Treating PCOS in Adolescents

To exam in the effect of a combination of low dose Metformin and Spironolactone on functional brain MRI, menstrual regulation and metabolism in adolescents with PCOS.

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Key information

Conditions

Age range

13 year–21 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Children's Mercy Hospital

Kansas City, Missouri, 64108, United States

About this study

Polycystic Ovarian Syndrome (PCOS) is the most common endocrinopathy in adolescent females and also one of the most complex. Patients experience an exaggerated ovarian/adrenal androgen production in response to physiologic and supra-physiologic elevations in insulin. The hormonal dysregulation is not only associated with acne, hirsutism, and menstrual irregularity, but also with perpetuated insulin resistance, central adiposity, and clinical depression.

In the proposed study, we aim to treat a hormonally and metabolically well-defined group of adolescent girls with PCOS with a combination of two pharmacological agents: metformin (insulin sensitizer) and spironolactone (anti-androgen) for 6 months. Although hyperandrogenism is a fundamental component of PCOS and responsible for the perpetuation of insulin resistance, adiposity and anovulation, there are few pediatric studies that have examined the benefits of treating both insulin resistance and hyperandrogenism simultaneously. Preliminary studies in adults, however, suggest synergistic effect of both spironolactone and metformin (spiro-met) with near normalization of the metabolic and ovulatory dysfunction. Therefore, we hypothesize that spiro-met will improve adolescent metabolism, body composition, ovarian morphology/function. We anticipate that our study will generate key pilot data for further randomized, double blind placebo controlled trials using both agents.

We also plan to examine functional brain MRI before and after the spiro-met intervention. This will allow us to inspect the effects of the hyperinsulinemic/androgenic hormonal milieu in PCOS on structural and functional brain MRI. We hypothesis, that the hormonal environment in PCOS affects centers of appetite and mood.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Generally healthy
  • Meeting Androgen Excess Society (AES) diagnostic criteria of PCOS: Menstrual Dysfunction or PCO ovaries on ultrasound AND clinical or biochemical hyperandrogenism
  • Normal liver and kidney function
  • No chronic illnesses except for stable, treated hypothyroidism

Exclusion criteria

  • Use of metformin and/or spironolactone within the last 6 months
  • Currently on either oral hormonal contraception or other forms of hormonal contraception such as Depo-Provera, NuvaRing
  • Current or past pregnancy
  • Currently sexually active
  • Psychiatric disorder based on self/parental report
  • Type 2 diabetes (blood glucose > 200mg/dl on OGTT)
  • Anemia (Hct < 35)
  • Impaired kidney function (Baseline creatinine > 1.0 mg)
  • Abnormal liver transaminases > 2 x the upper limit of normal range
  • Potassium elevated outside the reference range (in non-hemolyzed blood sample)

Treatment and study plan

Metformin and Spironolactone

Drug

Oral Metformin tablet (500 mg/tablet) twice daily for 6 months. Oral Spironolactone tablet (50 mg/tablet) once daily for 6 months.

Primary outcomes

  1. Oral Glucose Tolerance Test

    Time frame: Change Measures: Baseline & 6 Months

    Measurement of glucose and insulin at baseline and 2 hours after 75g of glucola.

  2. Total Testosterone

    Time frame: Change Measures: Baseline & 6 Months

    Total Testosterone measured in ng/dL

  3. Free Testosterone

    Time frame: Change Measures: Baseline & 6 Months

    Free Testosterone measured in ng/dL

  4. Dehydroepiandrosterone Sulfate (DHEAS)

    Time frame: Change Measures: Baseline & 6 Months

    DHEAS measured in mcg/dL

  5. Body Mass Index (BMI)

    Time frame: Change Measures: Baseline & 6 Months

    Body Mass Index measured in kg/m2

Sponsors and collaborators

Lead sponsor

Children's Mercy Hospital Kansas City

Other

Registry information

Important dates

Study start
2016
Primary completion
2018
Study completion
2019
First posted
Jun 11, 2019
Registry last updated
Feb 23, 2021

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.

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