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Low Dose OC Therapy in Women With Polycystic Ovary Syndrome (PCOS): Impact of BMI on Hyperandrogenism (BEYAZ-PCOS)

Primary Purpose

Polycystic Ovary Syndrome

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
3 mg DRSP/20 μg EE
Sponsored by
Woman's
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring PCOS

Eligibility Criteria

16 Years - 35 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • •Adult female-16 years to 35 years of age who have been diagnosed with PCOS desiring contraception

    • Actual BMI >18 to <35kg/ m2
    • Written consent for participation in the study
    • Patient completed lactation

Exclusion Criteria:

  • Metabolic abnormalities requiring pharmacological intervention (except controlled thyroid disease)

    • Uncontrolled hypertension
    • Cancer or history of hormone-dependent cancer
    • History of cholestasis
    • Presence of contradictions for OC administration
    • Personal history of cardiovascular events.
    • Use of drugs known to exacerbate glucose tolerance.
    • No prescription or over-the-counter weight-loss drugs
    • Diabetes
    • Use of medications that affect blood pressure or lipid profile
    • Smoking in past 6 months
    • Known thrombogenic mutations (e.g. Factor V Leiden)
    • Current or history of deep venous thrombosis/pulmonary embolism
    • Major surgery with prolonged immobilization
    • Injectable hormonal contraceptive use within 6 months
    • Use of hormonal (e.g., oral contraceptive [OC] pill) or insulin-sensitizing medication unless willing to cease medications for 3 months before study measurements

Sites / Locations

  • Woman's Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

3 mg DRSP/20 μg EE--normal weight

3 mg DRSP/20 μg EE- Overweight

3 mg DRSP/20 μg EE- Grade 1 obese

Arm Description

Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive Normal weight -BMI 18-24.9 kg/ m2

Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 25-29.9 kg/ m2

Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 30-34.9 kg/ m2

Outcomes

Primary Outcome Measures

Biochemical Assessment of Hyperandrogenism
The primary outcome measure is post-treatment Free Androgen Index(FAI) which is expressed in units. FAI is calculated by taking the testosterone concentration (in nmol/l) and dividing by concentration of sex hormone binding globulin (SHBG in nmol/L)and multiplying by 100

Secondary Outcome Measures

Cardiometabolic Measures
Values represent blood pressure at 24 weeks.
Post Therapy BMI.
Post-treatment body mass index at 24 weeks
Biochemical Indicator of B-vitamin Status
Post-treatment in folate concentrations after 24 weeks of treatment
Menstrual Cycle Regularity
Post treatment menstrual frequency over 24 weeks normalized to number of menses per year ..
Adrenal Androgen DHEAS
Post-treatment levels of adrenal androgen DHEAS
Oral Disposition Index
Post-treatment insulin secretion-sensitivity index (ISSI) calculated from the oral glucose tolerance test (OGTT). A higher value indicate improved carbohydrate metabolism

Full Information

First Posted
May 25, 2011
Last Updated
March 30, 2017
Sponsor
Woman's
Collaborators
Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma
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1. Study Identification

Unique Protocol Identification Number
NCT01360996
Brief Title
Low Dose OC Therapy in Women With Polycystic Ovary Syndrome (PCOS): Impact of BMI on Hyperandrogenism
Acronym
BEYAZ-PCOS
Official Title
Positive Clinical and Hormonal Effects of Ethinylestradiol Combined With Drospirenone (EE/DRSP) in Women With Polycystic Ovary Syndrome (PCOS): Impact of Body Weight and Relevance to Hyperandrogenism
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Woman's
Collaborators
Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The classic description of polycystic ovary syndrome (PCOS) is that it is a disorder characterized by menstrual irregularity, chronic anovulation, androgen excess, and abnormal gonadotropin secretion. Use of combined oral contraceptives (OCs) in women with PCOS effectively reduces circulating androgens. Although OCs are the most common and one of the oldest symptomatic treatment modalities for androgenic skin symptoms and for irregular menstrual cycles caused by hyperandrogenism, the data concerning the effect of treatment of PCOS women with different body mass index (BMI) are limited. This study is being done to compare the hormone and metabolic changes after treatment with low-dose oral birth control regimen of DRSP 3 mg/EE 0.02mg/levomefolate calcium 0.451 mg (Beyaz™) in women with PCOS with different body weights.
Detailed Description
Clinically, polycystic ovary syndrome (PCOS) is a heterogeneous disorder of functional androgen excess and the features of PCOS can run through a spectrum of severity. The optimal modality for long-term treatment of PCOS should positively influence androgen synthesis, sex hormone binding globulin (SHBG) production, insulin sensitivity, the lipid profile, and clinical symptoms including hirsutism and irregular menstrual cycles. Combined oral contraceptives have been a key component of the chronic treatment of women with PCOS; improving androgen excess and regulating menstrual cycles. The effect of OCs on ovarian folliculogenesis significantly decreases androgen production. This mechanism was confirmed in both healthy women and women with PCOS. In obese patients with PCOS, it is likely that the suppression of androgen production is not as significant. It is thus possible to hypothesize that the effects of OCs in PCOS could be dependent on body weight and what is needed is a head-to-head comparison. The aim of this study is to compare the effect of 6 months of a low-dose oral contraceptive regimen of 24/4 DRSP 3 mg/EE 0.02mg/levomefolate calcium 0.451 mg on androgen profiles, cardiometabolic measures, B-vitamin status, and menstrual cycle regulation in three groups, normal (BMI 18-24.9 kg/ m2) overweight (BMI 25-29.9 kg/ m2) and obese (BMI 30-35 kg/ m2) women with PCOS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
PCOS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
3 mg DRSP/20 μg EE--normal weight
Arm Type
Experimental
Arm Description
Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive Normal weight -BMI 18-24.9 kg/ m2
Arm Title
3 mg DRSP/20 μg EE- Overweight
Arm Type
Experimental
Arm Description
Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 25-29.9 kg/ m2
Arm Title
3 mg DRSP/20 μg EE- Grade 1 obese
Arm Type
Experimental
Arm Description
Folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive BMI 30-34.9 kg/ m2
Intervention Type
Drug
Intervention Name(s)
3 mg DRSP/20 μg EE
Other Intervention Name(s)
folate-boosted 3 mg DRSP/20 μg EE-24/4 oral contraceptive, BeYaz
Intervention Description
1 pill daily-24 days of drospirenone 3 mg (3 mg DRSP)/ethinyl estradiol 20 μg (20 μg EE)/levomefolate calcium 0.451 mg (folate) -followed by 4 days of levomefolate calcium 0.451 mg (folate)only
Primary Outcome Measure Information:
Title
Biochemical Assessment of Hyperandrogenism
Description
The primary outcome measure is post-treatment Free Androgen Index(FAI) which is expressed in units. FAI is calculated by taking the testosterone concentration (in nmol/l) and dividing by concentration of sex hormone binding globulin (SHBG in nmol/L)and multiplying by 100
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Cardiometabolic Measures
Description
Values represent blood pressure at 24 weeks.
Time Frame
24 weeks
Title
Post Therapy BMI.
Description
Post-treatment body mass index at 24 weeks
Time Frame
24 weeks
Title
Biochemical Indicator of B-vitamin Status
Description
Post-treatment in folate concentrations after 24 weeks of treatment
Time Frame
24 weeks
Title
Menstrual Cycle Regularity
Description
Post treatment menstrual frequency over 24 weeks normalized to number of menses per year ..
Time Frame
24 weeks
Title
Adrenal Androgen DHEAS
Description
Post-treatment levels of adrenal androgen DHEAS
Time Frame
24 weeks
Title
Oral Disposition Index
Description
Post-treatment insulin secretion-sensitivity index (ISSI) calculated from the oral glucose tolerance test (OGTT). A higher value indicate improved carbohydrate metabolism
Time Frame
24 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: •Adult female-16 years to 35 years of age who have been diagnosed with PCOS desiring contraception Actual BMI >18 to <35kg/ m2 Written consent for participation in the study Patient completed lactation Exclusion Criteria: Metabolic abnormalities requiring pharmacological intervention (except controlled thyroid disease) Uncontrolled hypertension Cancer or history of hormone-dependent cancer History of cholestasis Presence of contradictions for OC administration Personal history of cardiovascular events. Use of drugs known to exacerbate glucose tolerance. No prescription or over-the-counter weight-loss drugs Diabetes Use of medications that affect blood pressure or lipid profile Smoking in past 6 months Known thrombogenic mutations (e.g. Factor V Leiden) Current or history of deep venous thrombosis/pulmonary embolism Major surgery with prolonged immobilization Injectable hormonal contraceptive use within 6 months Use of hormonal (e.g., oral contraceptive [OC] pill) or insulin-sensitizing medication unless willing to cease medications for 3 months before study measurements
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen E Elkind-Hirsch, M.Sc.,Ph.D.
Organizational Affiliation
Woman's Hospital, Louisiana
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Martha Paterson, M.D.
Organizational Affiliation
Woman's Hospital Metabolic Health Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Woman's Hospital
City
Baton Rouge
State/Province
Louisiana
ZIP/Postal Code
70815
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Low Dose OC Therapy in Women With Polycystic Ovary Syndrome (PCOS): Impact of BMI on Hyperandrogenism

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