๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-13

Investigations of Reproductive Cancers in Women (NCT06527157)

PROspective ACcrual To Investigate reprOductive Cancers in womeN

๐ŸŸข Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: PinkDx, Inc.

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

The goal of this study is to create a non-invasive diagnostic test to rule out gynecological cancer in females aged 45 and older with abnormal uterine or postmenopausal bleeding.

Who can join: Review the eligibility criteria below.

Location: University of Alabama, Birmingham โ€” Birmingham, Alabama

Age range: 45 Years to 100 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (16 Sites)

  • University of Alabama, Birmingham โ€” Birmingham, Alabama
  • Sutter Health โ€” San Carlos, California
  • Advent Health Orlando โ€” Orlando, Florida
  • Ob-Gyne Associates of Lake Forest, Ltd โ€” Lake Forest, Illinois
  • Indiana University, Eskenazi Health โ€” Indianapolis, Indiana
  • Mayo Clinic โ€” Rochester, Minnesota
  • Washington University School of Medicine โ€” St Louis, Missouri
  • Columbia University โ€” New York, New York
  • Summa Health โ€” Akron, Ohio
  • The Ohio State University โ€” Columbus, Ohio
  • Avera Research Institute โ€” Sioux Falls, South Dakota
  • University of Tennessee Health Science Center โ€” Memphis, Tennessee
  • Meharry Medical College โ€” Nashville, Tennessee
  • Baylor College of Medicine/Texas Children's Hospital โ€” Houston, Texas
  • Houston Methodist โ€” Houston, Texas
  • University of Texas Health Science Center at San Antonio โ€” San Antonio, Texas

๐Ÿ“ž Contact the Study Coordinator

Phone: (463) 273-7024

Email: devon@pinkdx.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Uterine Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—