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(PCOS)

Polycystic Ovary Syndrome Research Study

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Do you have PCOS?

You’re invited to help Penn State Health and Penn State College of Medicine researchers discover how a nutritional supplement called Inositol can help manage polycystic ovary syndrome (PCOS) symptoms.

Compensation provided.

Study Overview

Who Can Volunteer

  • Women ages 18-45

  • Diagnosed with polycystic ovary syndrome (PCOS)

  • Able to travel to Penn State Health in Hershey, Pa., for study visits

  • Are not seeking pregnancy

  • Additional criteria may apply

What Volunteers Will Do

If you are eligible, you will be asked to complete some of the following activities in this study:

  • Have a physical exam and other evaluations, including ultrasound

  • Take the study drug as directed

  • Have bloodwork taken throughout the study

  • Complete questionnaires and keep a daily diary

This study will last a total of four months, and compensation is provided.

Keeping Volunteers Safe

We are taking several steps to keep research volunteers safe. This includes:

  • Conducting phone screening prior to scheduling visits

  • Using appropriate personal protective equipment (masks, face shields, gloves) during in-person research visits

  • Sanitation of all research spaces and equipment

Study Details

Finding alternatives to managing PCOS

Dr. Richard Legro and his study team are passionate about finding ways to help women with polycystic ovary syndrome (PCOS) manage their symptoms. Research is an important part of discovering new treatments and solutions for PCOS. This study, also known as INSUPP-PCOS, will see if a nutritional supplement called Inositol can help manage reproductive hormones and glucose tolerance in women with PCOS. When you participate in INSUPP, you will be randomly assigned to one of the groups below. Your group assignment is by chance, much like the flip of a coin.

  • Group 1: Will receive 2 grams of Inositol per day

  • Group 2: Will receive 4 grams of Inositol per day

  • Group 3: Will receive 6 grams of Inositol per day

  • Group 4: Will receive a placebo over a three-month period.

A placebo is not a drug and has no active ingredients. This is sometimes called a “sugar pill.” The placebo group will be compared to the other groups taking Inositol and will help researchers understand whether Inositol is effective. All groups will be asked to visit the study team in Hershey, Pa., to complete activities such as physical exams, laboratory assessments, ultrasound and bone density scans. Compensation is provided for participating in this study.

Meet the Study Director

Richard Legro stands beside a screen with a sonogram wearing a white lab coat

Chair, Department of Obstetrics and Gynecology

Richard S. Legro, MD

Dr. Richard Legro is has a long-standing interest in all aspects of polycystic ovary syndrome (PCOS), the most common endocrinopathy in women. His studies have focused on the diagnosis, treatment and genetic/environmental causes of PCOS, as well as on improving infertility diagnosis and treatment. He has worked with multiple clinical trial/research groups to develop novel and important investigator-initiated, multi-center trials to answer clinical questions about the role of lifestyle modification, medical agents and surgery to improve human reproductive function and treat infertility. Through these studies, Dr. Legro has pioneered the tracking of outcomes in mothers from preconception through pregnancy to the postpartum period, and infants from birth onward.

Explore More About Dr. Legro's ResearchchevronRight icon

For More Information

If you have any questions or are interested in participating, please contact the study coordinator, Amyee McMonagle:

Polycystic Ovary Syndrome (PCOS) Research Study

Amyee McMonagle

This research has been approved by the Institutional Review Board, under federal regulations at Penn State Health Milton S. Hershey Medical Center and Penn State College of Medicine as IRB #10252.