Obesity and Hormone Response Study in Women

Convergent Mechanisms Underlying Reprometabolic Syndrome in Women

Recruiting Phase 2 Interventional Study
Infertility, Female Obesity
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 38
Sex
Female
Trial phase
Phase 2
Study type
Interventional
Purpose
Basic Science
Participants needed
20 (estimated)
Sponsor
University of Colorado, Denver · Other
Who this trial is looking for

This trial is looking for women aged 18-38 who have regular menstrual cycles and are not using reproductive hormones. Participants will take part in research to understand how obesity affects hormone responses related to fertility.

Are You a Good Fit for This Trial?
Rules you out DiabetesVenous thromboembolism

You may be able to join if

  • I am aged 18-38
  • I have regular menstrual cycles every 25-35 days
  • I have not used reproductive hormones in the past 3 months
  • I have not taken medications that affect reproductive hormones
  • I agree to use reliable barrier contraception or abstain from intercourse
  • My thyroid stimulating hormone, prolactin, and lipid profiles are normal
  • I exercise moderately for no more than 4 hours a week
  • I have no history of chronic diseases affecting reproductive hormones

You may not be able to join if

  • I have diabetes
  • I smoke
  • I have a history of blood clots or known blood clotting disorders

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

Dr. Nanette Santoro proposes to test the specific question that obesity results in abnormal estradiol response at the level of the pituitary and hypothalamus. This will be shown in diminished pituitary sensitivity to gonadorelin releasing hormone with a reduced estradiol induced luteinizing hormone surge in obese women.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18-38 * Regular menstrual cycles every 25-35 days * No use of reproductive hormones within the past 3 months * No use of medications interacting with reproductive hormones * Agreement to use reliable barrier contraception or to abstain from intercourse for the duration of …
Contacts

Carrie Hsu

303-724-5276

Carire.Hsu@cuanschutz.edu

CONTACT

Asma Giornazi

asma.giornazi@cuanschutz.edu

CONTACT