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Polycystic Ovary Syndrome (PCOS)NCT01927471

Nutritional and Metabolic Correlates of Ovarian Morphology in Women With Polycystic Ovary Syndrome

An observational study of Polycystic Ovary Syndrome (PCOS) and Menstrual Irregularity, run by Cornell University at 3 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The investigators would like to determine how aspects of metabolism and age influence ovarian function. The purpose of the study is to understand how nutrition and metabolism relate to follicle development in women with regular cycles, irregular cycles, or polycystic ovary syndrome (PCOS). Read more about this study

Who is it for?
Ages 18 to 48 years, women onlyHealthy volunteers can take part
How many people
129 participants
Where
3 sitesUnited States
Study dates
Sep 2011to Jul 2019
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 48 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Study population: Women must be able to transport to Cornell University and University of Rochester. Eligible participants are between 18-48 years with a BMI of 18 kg/m2 or higher. Women are screened and enrolled following consent based on their response to our advertisements. Enrollment is restricted to the geographical area.

Who may be able to join

  • Between 18 and 48 years
  • BMI ≥ 18 kg/m2
  • Either:
  • Regular menstrual cycles (21-35 days);
  • Irregular menstrual cycles (>36 days); or
  • Previous diagnosis of PCOS from a primary care provider
  • If 21 years of age or older, must have had a healthy pelvic exam w/in the past 2 years

Who cannot join

  • Current use of medication(s) known or suspected to interfere with reproductive function (eg. oral contraceptives) or insulin sensitivity
  • Pregnant or breastfeeding
  • Not otherwise healthy
  • Significant weight changes within the last three months

Trial locations and contacts

3 sites in 1 country.

United States3 sites
  • Human Metabolic Research Unit, Cornell University

    Ithaca, New York, 14853

  • Strong Fertility Center

    Rochester, New York, 14623

  • CRC at University of Rochester Medical Center

    Rochester, New York, 14642

Other trials in United States

About this study

The investigators would like to determine how aspects of metabolism and age influence ovarian function. The purpose of the study is to understand how nutrition and metabolism relate to follicle development in women with regular cycles, irregular cycles, or polycystic ovary syndrome (PCOS). We also plan to identify lifestyle factors associated with PCOS and understand how diet and activity levels impact features of PCOS.

Read the detailed description

In the ovaries, eggs rest in fluid filled sacs called follicles. When follicles grow they form small fluid-filled cysts that can be easily seen when we use ultrasound to view the ovaries. In women with regular menstrual cycles, groups of follicles grow and regress 2 to 3 times during their cycle (usually over a 28- day period). Several of these follicles grow to a stage where they begin to develop the potential to ovulate - but in general only one follicle is chosen to ovulate. Thus, at any given time during the menstrual cycle, numerous fluid-filled follicles can be visualized in a woman's ovaries at various stages of development using transvaginal ultrasonography. In women with absent or infrequent menstrual cycles, very little is known about the growth patterns of their follicles and how factors such as metabolic hormones, might play a role in the failure to ovulate. Being underweight or overweight increases your chances of having irregular or absent menstrual cycles and a history of abnormal reproductive function compounds your risks for chronic diseases such as infertility, diabetes, hypertension, atherosclerosis and certain cancers. This is particularly the case for women with PCOS that have menstrual cycles that appear to worsen or improve depending on their body weight and metabolic status. Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects 6-12% of reproductive-aged women within the general population. The hallmark features of PCOS are menstrual irregularity, increased levels of androgens, and polycystic ovaries. The current diagnostic criteria require 2 out of 3 of these features to be present for the diagnosis, therefore a number of phenotypes of PCOS exist. However, the metabolic and reproductive differences across the phenotypic spectrum of PCOS are not well understood. Women with PCOS characteristically have polycystic ovaries, where up to 10 times more follicles are present in the ovary at any given time. Further, the follicle-size populations and overall distribution throughout the ovary varies in women - follicles may be situated around the periphery of the ovary or may be distributed throughout the ovary. Presumably these small follicles are arrested in development - but emerging data from the Lujan laboratory suggest that this is not the case. Rather, follicles continue to grow in a dynamic pattern during these prolonged periods of anovulation. By comparing follicle populations, reproductive hormones and markers of metabolism in women with regular cycles, women with irregular cycles, and women with a history of PCOS, the researchers plan to identify what factors might explain why fertility potential and long-term health are compromised in some women but not in others. By including women at both early and late stages of their reproductive potential, the researchers will also be able to assess what influence age has on these factors. The ultimate goal of this research is to understand how nutrition and metabolism regulate follicle development in women so we can better develop lifestyle and drug therapies to help women preserve their fertility and long-term health. Since obesity has recently become the leading cause of infertility in North America, these studies are especially important.

Current research has failed to thoroughly examine the relationships between dietary intake, energy expenditure and PCOS. The purpose of this proposed study is to identify lifestyle factors associated with PCOS. Through dietary intake and energy expenditure data, the researchers plan to examine potential lifestyle differences between PCOS and healthy women, as well as between BMI classifications within women with PCOS. The Research Team will also be able to evaluate the diet quality according to the USDA Dietary Guidelines for Americans of all women included in the study. The Research Team is also interested in the relationships between biological markers and lifestyle endpoints in women with and without PCOS. Previous literature has shown there are biological marker differences between those with and without PCOS. By examining these relationships, researchers may further understand whether PCOS status is associated with lifestyle parameters.

To accomplish these objectives, the investigators plan to recruit 120 women with regular menstrual cycles and 240 women with irregular menstrual cycles, with or without PCOS (sub-grouped into 120 women with irregular menstrual cycles and 120 women with a history of PCOS). Their goal is to recruit an equal number of women in each group such that they are matched for age (18 - 48 years old) and body mass index (BMI; Normal weight = 18 - 24.9 kg/m2; Overweight = 25 - 29.9 kg/m2; Obese ≥ 30kg/m2). Women will be included in the PCOS sub-group if they have a confirmed PCOS diagnosis from their primary care provider. Ultrasound scans of the ovaries will be assessed for the total number, size, and distribution of follicles using both two- and three-dimensional imaging techniques. Participants will have blood samples collected determine serum concentrations of luteinizing hormone (LH), follicle stimulating hormone (FSH), estradiol, progesterone, anti-müllerian hormone (AMH), and inhibin B. The following metabolic parameters will be assessed: (1) 75-gram oral glucose tolerance test to characterize glucose and insulin dynamics at 0, 30, 60, 90, and 120 minutes post-glucose ingestion; (2) dual X-ray absorptiometry (DXA) scan to quantify body fat and lean muscle distribution; (3) vitals and anthropometry assessment to measure waist and hip circumference, height, weight, blood pressure, and heart rate, and (4) fasting blood tests to detect serum concentrations of androgens (i.e., total testosterone, androstenedione, free androgen index) and serum markers of metabolic syndrome (i.e., lipids and hemoglobin A1C). Participants will complete a food frequency questionnaire, a semi-structured dietary interview, and physical activity questionnaire. A researcher may also provide participants with an accelerometer to wear for a week. Participants may also elect to participate in an optional subcutaneous fat biopsy.

Keywords
Menstrual cycles, Ultrasound, Ovary, Polycystic Ovary Syndrome (PCOS), Physical activity, Diet
Medical subject headings
Polycystic Ovary Syndrome, Menstruation Disturbances, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01927471
Study groupRoleWhat they receive
Regular menstrual cyclesAdult women will be assigned to this category if they report a history of regular menstrual cycles. We will aim to recruit 120 women in this category.
Irregular menstrual cycles, no PCOSAdult women will be assigned to this category if they report a history of irregular menstrual cycles, without a pre-existing diagnosis of PCOS. We will aim to recruit 120 women in this category.
Irregular menstrual cycles, with PCOSAdult women will be assigned to this category if they report a history of irregular menstrual cycles with a pre-existing diagnosis of PCOS by a physician. We will aim to recruit 120 women in this category.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Follicle number per ovary

    The number and size of all follicles in each ovary will be assess by ultrasonography for each participant with regular menstrual cycles, irregular menstrual cycles and PCOS.

    Measured: 1 day

  2. Insulin sensitivity

    Insulin sensitivity will be determined by administration of an oral glucose tolerance test and compared across groups.

    Measured: 1 day

Secondary outcomes (14)
  1. Ovarian Volume

    The size of each ovary will be determined by ultrasonography for each participant and compared across groups.

    Measured: 1 day

  2. Anti-Müllerian hormone

    Circulating AMH levels in the serum will be determined for each participant and compared across groups.

    Measured: 1 day

  3. LH-FSH ratio

    The ratio of circulating LH to FSH concentrations in the serum will be determined for each participant and compared across groups.

    Measured: 1 day

  4. Androgen concentrations

    Total testosterone, androstenedione and free androgen index concentrations in serum will be determined and compared across groups.

    Measured: 1 day

  5. Menstrual Cycle Length

    Average menstrual cycle length as determined by self-reported history will be determined and compared across groups.

    Measured: 1 day

  6. Hirsutism

    Degree of hirsutism as judged by the Ferriman-Gallwey scale will be determined and compared across groups.

    Measured: 1 day

  7. Serum markers of metabolic syndrome

    Lipids, glucose and HbA1C concentrations will be determined and compared across groups.

    Measured: 1 day

  8. Blood Pressure

    Blood pressure will be determined and compared across groups.

    Measured: 1 day

  9. Body mass index

    The ratio of weight to height will be determined and compared across groups.

    Measured: 1 day

  10. Waist-to-hip ratio

    The ratio of waist circumference to hip circumference will be determined and compared across groups.

    Measured: 1 day

  11. Body fat distribution

    Percentage and distribution of fat and lean mass as assessed using DXA technology will be compared across groups.

    Measured: 1 day

  12. Differences in diet composition between women with and without PCOS

    A food frequency questionnaire will be administered to assess diet composition for the last three months

    Measured: 1 week

  13. Differences in energy expenditure between women with and without PCOS

    Participants will be asked to wear a small accelerometer device to assess physical activity

    Measured: 1 week

  14. Subcutaneous fat biopsy (optional)

    Subcutaneous fat biopsies will be conducted to assess differences in fat cell populations (major site of reproductive hormone synthesis) between groups

    Measured: 1 day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Aug 2013 (estimated)
  2. Study startSep 2011
  3. Primary completionJul 2019
  4. Study completionJul 2019

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
129 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01927471
Sponsor's protocol ID
IRB #: 1108002383
Status last verified
Feb 2024
First submitted
20 Aug 2013
Last updated
9 Feb 2024
Results posted
No
Data monitoring committee
No

Publications

  • Evans AT, Rehani E, Smith B, Hong MD, Lewin Z, Hiroshige K, Spandorfer SD, Hajirasouliha I, Lujan ME, Hoeger KM. Diagnosis of Polycystic Ovary Syndrome With Predictive Modeling of Select Clinical Features. O G Open. 2026 Mar 19;3(2):e161. doi: 10.1097/og9.0000000000000161. eCollection 2026 Apr.

    PubMed 41868592

Questions about this trial

What is this clinical trial studying?

An observational study of Polycystic Ovary Syndrome (PCOS) and Menstrual Irregularity, run by Cornell University at 3 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Follicle number per ovary (time frame: 1 day). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01927471, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Feb 2024.

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