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Mechanisms of Increased Androgen Production Among Women With Polycystic Ovary Syndrome

Primary Purpose

Polycystic Ovary Syndrome

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
3-D Ultrasound
recombinant human chorionic gonadotropin
Recombinant human follicle stimulating hormone
Adrenocorticotropin
Dexamethasone
Glucose
Sponsored by
University of California, San Diego
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Polycystic Ovary Syndrome focused on measuring PCOS, Androgens, ovary, polycystic

Eligibility Criteria

18 Years - 37 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

A group of 40 women with PCOS and 20 normal women ages 18-37 will be studied.

  • Subjects will be determined to have PCOS based on clinical history of irregular menses and clinical or laboratory evidence of hyperandrogenism and polycystic ovaries on ultrasound.
  • Subjects should not have been on any hormonal therapy or metformin for at least 2 months prior to study start.
  • Subjects will be determined to be normal controls if they have a clinical history of regular periods

Exclusion Criteria:

  • Women with hemoglobin less than 11 gm/dl at screening evaluation
  • Women with untreated thyroid abnormalities
  • Pregnant women or women who are nursing
  • Women with BMI > 37
  • Women with known sensitivity to the agents being used
  • Women with prosthetic devices (i.e.,ear)/ shunts (ventricular), Hearing aids, Metal plate/pins/screws/wires
  • Women with diabetes, or renal, liver, or heart disease.

Sites / Locations

  • UCSD Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

PCOS women

Normal women

Arm Description

Each subject will undergo pelvic 3D ultrasound followed by an iv recombinant human chorionic gonadotropin (r-hCG) stimulation test. One month later the r-hCG test will be repeated 24 hr after an injection of recombinant human follicle stimulating hormone (FSH). After 1 month, subjects will receive a 7 hr dose-response infusion of adrenocorticotropin (ACTH) with blood sampling. Dexamethasone will be given prior to ACTH. After 1 month, subject will receive r-hCG as described above followed the next day by an oral glucose tolerance test (OGTT). Subsequently, subjects will take Diazoxide 3 times a day for 2 weeks. At weekly intervals (2 weeks), the r-hCG stimulation test will be repeated followed the next day by an OGTT as described above.

Each subject will undergo pelvic 3D ultrasound followed by an iv recombinant human chorionic gonadotropin (r-hCG) stimulation test. One month later the r-hCG test will be repeated 24 hr after an injection of recombinant human follicle stimulating hormone (FSH). After 1 month, subjects will receive a 7 hr dose-response infusion of adrenocorticotropin (ACTH) with blood sampling. Dexamethasone will be given prior to ACTH. After 1 month, subject will receive r-hCG as described above followed the next day by an oral glucose tolerance test (OGTT). Subsequently, subjects will take Diazoxide 3 times a day for 2 weeks. At weekly intervals (2 weeks), the r-hCG stimulation test will be repeated followed the next day by an OGTT as described above.

Outcomes

Primary Outcome Measures

17-hydroxyprogesterone Responses to hCG in PCOS Women and Normal Controls
Change from baseline in 17-hydroxyprogesterone at 24 hours after hCG injection

Secondary Outcome Measures

Adrenal 17-hydroxyprogesterone Response to ACTH in PCOS Women and Normal Controls
17-hydroxyprogesterone response to ACTH infusion in women with PCOS and normal women. Response is reported as a single value generated by summing the data at end time frame.
17 Hydroxyprogesterone Response to hCG Injection After Lowered Insulin Levels.
17 hydroxyprogesterone levels
Anti-Mullerian Hormone (AMH)

Full Information

First Posted
October 5, 2009
Last Updated
May 1, 2018
Sponsor
University of California, San Diego
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1. Study Identification

Unique Protocol Identification Number
NCT00989781
Brief Title
Mechanisms of Increased Androgen Production Among Women With Polycystic Ovary Syndrome
Official Title
Mechanisms of Increased Androgen Production Among Women With Polycystic Ovary Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Diego

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Jeffrey Chang MD is conducting a research study to learn more about the increased male hormone levels, otherwise known as androgens, seen in women with polycystic ovary syndrome (PCOS). Women with PCOS have ovaries that are comprised of many cysts, or follicles. They also have irregular or absent menstrual periods and symptoms of increased male hormones, such as facial hair or acne. In each part of the study (except part 4 which is for PCOS women only) we will be comparing responses of PCOS women to normal controls
Detailed Description
The first part of this study looks specifically at the structure of the ovaries, which are the female sex glands where both androgens and estrogens (female hormones) are made. It involves imaging your ovaries with a technology called 3-D Ultrasound. We are interested in recording the number, size and arrangement of the follicles in your ovaries. The second part of the study looks at how the ovary produces male hormones, or androgens, with and without follicle stimulating hormone (FSH) stimulation. Hormones are substances made by a gland in one part of the body which regulate another part. FSH is a hormone naturally produced by the pituitary gland located in the brain and it helps the ovary produce estrogens, or female hormones. LH is a hormone also naturally produced by the pituitary gland and it has the ability to stimulate the ovary to make androgens. We are interested to see how much androgen your ovaries will produce in response to LH with and without FSH. To accomplish this, you will be given FSH as well as hCG, a drug that acts like LH to stimulate the ovary; FSH and hCG are approved by the Food and Drug Administration (FDA) for this investigational, off-label use. The third part of the study looks at how much the adrenal glands contribute to the increase male hormone levels seen in PCOS. ACTH is a hormone naturally produced by the pituitary gland located in the brain and it stimulates the adrenals to make hormones. The adrenal glands are above the kidneys. They are chiefly responsible for helping the body adjust to stressful situations and work by producing cortisol and adrenaline. The adrenal glands also produce androgens, or male hormones. Previous studies have shown that some women with PCOS produce more male hormones from their adrenals. We are interested to see how much androgen your adrenal glands produce. To accomplish this, you will first be given dexamethasone, a stress steroid, to temporarily suppress your adrenal glands. You will then be given ACTH intravenously over the course of 7 hours to stimulate your adrenal glands. The fourth part of the study is for PCOS women only and looks at how much the role of insulin contributes to the increase male hormone levels. Insulin is a hormone naturally produced by the pancreas that stimulates all of the cells in your body to take up glucose, or sugar, from the blood. Previous studies have shown that PCOS women who are more resistant to insulin, or whose cells do not take up glucose from the blood in response to insulin, make more male hormones. We are interested to see how much androgen your ovaries produce in response to LH before and after we temporarily decrease the amount of insulin in your blood. To accomplish this, you will again be given hCG, a drug that acts like LH to stimulate the ovary, with and without diazoxide, a drug that decreases the amount of insulin in your bloodstream. These tests will all be done after you are on a diet that limits how much sugar you eat. To test how much insulin you make, you will also be given Oral Glucose Tolerance Tests before and after diazoxide. This test is done by drinking a sugary liquid and testing your blood over 3 hours.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
41 (Actual)

8. Arms, Groups, and Interventions

Arm Title
PCOS women
Arm Type
Experimental
Arm Description
Each subject will undergo pelvic 3D ultrasound followed by an iv recombinant human chorionic gonadotropin (r-hCG) stimulation test. One month later the r-hCG test will be repeated 24 hr after an injection of recombinant human follicle stimulating hormone (FSH). After 1 month, subjects will receive a 7 hr dose-response infusion of adrenocorticotropin (ACTH) with blood sampling. Dexamethasone will be given prior to ACTH. After 1 month, subject will receive r-hCG as described above followed the next day by an oral glucose tolerance test (OGTT). Subsequently, subjects will take Diazoxide 3 times a day for 2 weeks. At weekly intervals (2 weeks), the r-hCG stimulation test will be repeated followed the next day by an OGTT as described above.
Arm Title
Normal women
Arm Type
Experimental
Arm Description
Each subject will undergo pelvic 3D ultrasound followed by an iv recombinant human chorionic gonadotropin (r-hCG) stimulation test. One month later the r-hCG test will be repeated 24 hr after an injection of recombinant human follicle stimulating hormone (FSH). After 1 month, subjects will receive a 7 hr dose-response infusion of adrenocorticotropin (ACTH) with blood sampling. Dexamethasone will be given prior to ACTH. After 1 month, subject will receive r-hCG as described above followed the next day by an oral glucose tolerance test (OGTT). Subsequently, subjects will take Diazoxide 3 times a day for 2 weeks. At weekly intervals (2 weeks), the r-hCG stimulation test will be repeated followed the next day by an OGTT as described above.
Intervention Type
Radiation
Intervention Name(s)
3-D Ultrasound
Intervention Description
One time pelvic ultrasound
Intervention Type
Drug
Intervention Name(s)
recombinant human chorionic gonadotropin
Other Intervention Name(s)
Ovidrel, r-hCG
Intervention Description
Recombinant human chorionic gonadotropin will be given iv and blood samples obtained before and 24 hr afterwards
Intervention Type
Drug
Intervention Name(s)
Recombinant human follicle stimulating hormone
Other Intervention Name(s)
Gonal-F, r-hFSH
Intervention Description
Recombinant human follicle stimulating hormone will be given iv and blood samples obtained before and 24 hr later.
Intervention Type
Drug
Intervention Name(s)
Adrenocorticotropin
Other Intervention Name(s)
Cosyntropin, ACTH
Intervention Description
Each subject will receive a 7 hr dose-response infusion of Adrenocorticotropin.
Intervention Type
Drug
Intervention Name(s)
Dexamethasone
Other Intervention Name(s)
corticosteroid
Intervention Description
Dexamethasone will be given prior to ACTH infusion test.
Intervention Type
Drug
Intervention Name(s)
Glucose
Other Intervention Name(s)
sugar
Intervention Description
Each subject will undergo 3 oral glcuose tolerance tests.
Primary Outcome Measure Information:
Title
17-hydroxyprogesterone Responses to hCG in PCOS Women and Normal Controls
Description
Change from baseline in 17-hydroxyprogesterone at 24 hours after hCG injection
Time Frame
Baseline and 24 hours after hCG
Secondary Outcome Measure Information:
Title
Adrenal 17-hydroxyprogesterone Response to ACTH in PCOS Women and Normal Controls
Description
17-hydroxyprogesterone response to ACTH infusion in women with PCOS and normal women. Response is reported as a single value generated by summing the data at end time frame.
Time Frame
Baseline and 1, 2, 3, 4, 5, and 6 hours after ACTH
Title
17 Hydroxyprogesterone Response to hCG Injection After Lowered Insulin Levels.
Description
17 hydroxyprogesterone levels
Time Frame
Baseline and 24 after hCG
Title
Anti-Mullerian Hormone (AMH)
Time Frame
Baseline
Other Pre-specified Outcome Measures:
Title
Follicle Count on 3-D Ultrasound in PCOS Women and Normal Controls
Description
3-D ultrasound was not assessed; instead 2-D ultrasound was performed
Time Frame
baseline

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
37 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A group of 40 women with PCOS and 20 normal women ages 18-37 will be studied. Subjects will be determined to have PCOS based on clinical history of irregular menses and clinical or laboratory evidence of hyperandrogenism and polycystic ovaries on ultrasound. Subjects should not have been on any hormonal therapy or metformin for at least 2 months prior to study start. Subjects will be determined to be normal controls if they have a clinical history of regular periods Exclusion Criteria: Women with hemoglobin less than 11 gm/dl at screening evaluation Women with untreated thyroid abnormalities Pregnant women or women who are nursing Women with BMI > 37 Women with known sensitivity to the agents being used Women with prosthetic devices (i.e.,ear)/ shunts (ventricular), Hearing aids, Metal plate/pins/screws/wires Women with diabetes, or renal, liver, or heart disease.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R. Jeffrey Chang, M.D.
Organizational Affiliation
Professor
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCSD Medical Center
City
San Diego
State/Province
California
ZIP/Postal Code
92103
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Mechanisms of Increased Androgen Production Among Women With Polycystic Ovary Syndrome

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