Actively Recruiting

Age: 12Years - 80Years
FEMALE
Healthy Volunteers
NCT05797909

The PCOS Challenge Study

Led by PCOS Challenge: The National Polycystic Ovary Syndrome Association · Updated on 2023-04-04

15000

Participants Needed

1

Research Sites

1071 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary purpose of The PCOS Challenge Study will be to conduct high-quality research where patients are included in the design, and answering the questions that patients identify as important to their lived experience with PCOS. In partnership with clinical investigators, patients will work on the development and management of data collection, the research agenda, and the sharing of research findings. The PCOSC Study will promote the advancement of research that provides reliable, useful, and meaningful information to patients with PCOS and their clinicians. The population for The PCOS Challenge Study will include individuals with a clinical diagnosis of PCOS, individuals self-diagnosed with PCOS, individuals with symptoms of PCOS (e.g., hirsutism, irregular menstrual cycles), and demographic-matched controls without PCOS.

CONDITIONS

Official Title

The PCOS Challenge Study

Who Can Participate

Age: 12Years - 80Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with PCOS by a health professional, self-diagnosed with PCOS, or having symptoms of PCOS such as hirsutism or irregular menstrual cycles
  • Willing to sign the consent form
  • Able to understand the registry surveys or questions asked
Not Eligible

You will not qualify if you...

  • Unable to understand the surveys or questions asked
  • Unwilling to sign the consent form

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

PCOS Challenge: The National Polycystic Ovary Syndrome Association

Bethesda, Maryland, United States, 20817

Actively Recruiting

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Research Team

S

Sasha Ottey, MHA, MT (ASCP)

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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