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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Overall Study | Experimental | Treatment with Metformin and Spironolactone |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| 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. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Oral Glucose Tolerance Test | Measurement of glucose and insulin at baseline and 2 hours after 75g of glucola. | Change Measures: Baseline & 6 Months |
| Total Testosterone | Total Testosterone measured in ng/dL | Change Measures: Baseline & 6 Months |
| Free Testosterone | Free Testosterone measured in ng/dL | Change Measures: Baseline & 6 Months |
| Dehydroepiandrosterone Sulfate (DHEAS) | DHEAS measured in mcg/dL | Change Measures: Baseline & 6 Months |
| Body Mass Index (BMI) | Body Mass Index measured in kg/m2 | Change Measures: Baseline & 6 Months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Tania Burgert, MD | Children's Mercy Hospital Kansas City | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Children's Mercy Hospital | Kansas City | Missouri | 64108 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Overall Study | The pilot study was a non-controlled open label drug intervention study in a sample of adolescent girls attending a polycystic ovary syndrome (PCOS) clinic. Subjects received 6 months combination drug therapy with a combination of low dose metformin and spironolactone. |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Treatment | Treatment with Metformin and Spironolactone Metformin and Spironolactone: Oral Metformin tablet (500 mg/tablet) twice daily for 6 months. Oral Spironolactone tablet (50 mg/tablet) once daily for 6 months. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Oral Glucose Tolerance Test | Measurement of glucose and insulin at baseline and 2 hours after 75g of glucola. | Posted | Mean | Standard Deviation | mg/dL | Change Measures: Baseline & 6 Months |
|
|
adverse event data was collected for the duration of the subject's intervention: 6 months
Metformin is not known to cause death or hospitalization.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Overall Study | The pilot study was a non-controlled open label drug intervention study in a sample of adolescent girls attending a polycystic ovary syndrome (PCOS) clinic. Subjects received 6 months combination drug therapy with a combination of low dose metformin and spironolactone. |
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Early termination leading to small numbers of subjects analyzed; Technical problems with measurement leading to unreliable or uninterpretable data. Study was not published for this reason.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Tania Burgert | ChildrensMHC | 203 676 4545 | tsburgert@cmh.edu |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jan 17, 2019 | Dec 8, 2020 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D008687 | Metformin |
| D013148 | Spironolactone |
| ID | Term |
|---|---|
| D001645 | Biguanides |
| D006146 | Guanidines |
| D000578 | Amidines |
| D009930 | Organic Chemicals |
| D007783 |
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| years |
|
| Sex/Gender, Customized | Count of Participants | Participants |
|
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
|
| Race (NIH/OMB) | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| whole body insulin sensitivity index (WBISI) | WBISI does not have a lot of normative data to help categorize values. However, < 4.3 is deemed insulin resistant. The lower the number the more insulin resistant. | Mean | Standard Deviation | μU/ml |
|
| Body Mass Index (BMI) | Mean | Standard Deviation | kg/m2 |
|
|
| Primary | Total Testosterone | Total Testosterone measured in ng/dL | Posted | Mean | Standard Deviation | ng/dL | Change Measures: Baseline & 6 Months |
|
|
|
| Primary | Free Testosterone | Free Testosterone measured in ng/dL | Posted | Mean | Standard Deviation | ng/dL | Change Measures: Baseline & 6 Months |
|
|
|
| Primary | Dehydroepiandrosterone Sulfate (DHEAS) | DHEAS measured in mcg/dL | Posted | Mean | Standard Deviation | mcg/dL | Change Measures: Baseline & 6 Months |
|
|
|
| Primary | Body Mass Index (BMI) | Body Mass Index measured in kg/m2 | Posted | Mean | Standard Deviation | kg/m2 | Change Measures: Baseline & 6 Months |
|
|
|
| 0 |
| 12 |
| 0 |
| 12 |
| 0 |
| 12 |
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| Lactones |
| D011283 | Pregnenes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |