NCT01745471

Brief Summary

The purpose of this study is to collect data to help understand why some women develop Polycystic Ovary Syndrome (PCOS) associated with decreased lower-body fat.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
36

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Dec 2012

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 5, 2012

Completed
1 day until next milestone

Study Start

First participant enrolled

December 6, 2012

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 10, 2012

Completed
11.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 4, 2024

Completed
1.7 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

August 3, 2025

Status Verified

August 1, 2025

Enrollment Period

11.3 years

First QC Date

December 5, 2012

Last Update Submit

August 1, 2025

Conditions

Keywords

Abdominal AdiposeGluteal AdiposePolycystic Ovary SyndromeObesityWomen

Outcome Measures

Primary Outcomes (1)

  • Difference of angiogenesis capacity in abdominal and gluteal adipose tissue

    The angiogenesis capacity of each adipose tissue depot will be determine by an in vitro angiogenesis test.

    Day 7

Secondary Outcomes (2)

  • Presence of biomarkers in abdominal and gluteal adipose tissue in obese and PCOS women

    Day 7

  • Difference in oxygen content of abdominal and gluteal adipose tissue

    Day 6

Other Outcomes (2)

  • The rates of carbohydrate oxidation

    Day -7

  • The rates of lipid oxidation

    Day -7

Study Arms (3)

PCOS group

12 women with Polycystic Ovary Syndrome (PCOS) as defined by NIH criteria

Pear shapes

12 with an android pattern as defined by a waist-to-hip greater than 0.85

Apple shapes

12 will have a gynoid pattern as defined by a waist-to-hip ratio less than 0.78

Eligibility Criteria

Age20 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)
Sampling MethodProbability Sample
Study Population

Study Population and screening: Healthy young women with a BMI \> 30 will be recruited; 12 will have a gynoid pattern as defined by a waist-to-hip ratio less than 0.78 and 12 with an android pattern as defined by a waist-to-hip greater than 0.85. A third group will include 12 women with PCOS as defined by the NIH criteria. Subjects will be recruited via a dedicated website, physician referrals, direct mail outs, newspaper advertisements, and brochures. Only subjects that will sign informed consent and meet eligibility criteria will be enrolled in this study.

You may qualify if:

  • Female
  • Age \> 20 and \< 40
  • Weight stable (change of less than 3 kg in the last 8 weeks)
  • BMI \< 40 kg/m2 or \> 27 kg/m2
  • NIH criteria - confirmed by subjects' medical records.

You may not qualify if:

  • Male
  • Women who are pregnant or lactating (breast feeding)
  • Post-menopausal women
  • Women with hysterectomy
  • Diagnosed with diabetes, or have a fasting blood sugar \> 126 mg/dL.
  • Untreated or symptomatic thyroid disease.
  • Impaired kidney or liver function, as evidenced by your blood work
  • Hypertension/ high blood pressure or are taking blood pressure medications
  • Use of oral contraceptives or hormone replacement therapy.
  • History of drug or alcohol abuse (\> 3 drinks per day) in the last 5 years, or psychiatric disease prohibiting adherence to study protocol.
  • History of cancer within the last 5 years.
  • History of organ transplant.
  • History of HIV, active Hepatitis B or C, or Tuberculosis.
  • History of heart attack/ myocardial infarction.
  • Presence of clinically significant abnormalities on EKG.
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Translational Research Institute for Metabolism and Diabetes

Orlando, Florida, 32804, United States

Location

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Related Links

Biospecimen

Retention: SAMPLES WITH DNA

Blood Urine Adipose tissue

MeSH Terms

Conditions

Polycystic Ovary SyndromeMetabolic DiseasesOverweightObesity

Condition Hierarchy (Ancestors)

Ovarian CystsCystsNeoplasmsOvarian DiseasesAdnexal DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital DiseasesGonadal DisordersEndocrine System DiseasesNutritional and Metabolic DiseasesOvernutritionNutrition DisordersBody WeightSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Adeline Divoux, PhD

    Translational Research Institute for Metabolism and Diabetes

    PRINCIPAL INVESTIGATOR
  • Steven R Smith, MD

    Translational Research Institute for Metabolism and Diabetes

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 5, 2012

First Posted

December 10, 2012

Study Start

December 6, 2012

Primary Completion

April 4, 2024

Study Completion

December 1, 2025

Last Updated

August 3, 2025

Record last verified: 2025-08

Locations