๐๏ธ Verified NIH Record โข Updated 2026-08-13
Investigations of Reproductive Cancers in Women (NCT06527157)
PROspective ACcrual To Investigate reprOductive Cancers in womeN
๐ข Recruiting Interventional Protocol ๐ Observational Clinical Research Sponsor: PinkDx, Inc.
๐ฉบ 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
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ 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
๐ 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.
๐ฐ 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.
More studies in Uterine Cancer
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- Insights Into Participating in Studies for Uterine Cancer โ San Francisco, California
- Zanzalintinib in Combination With Paclitaxel in Recurrent High Grade Uterine Cancer โ San Francisco, California
- [18F]FES PET/.CT in Uterine Cancer โ Philadelphia, Pennsylvania
- Trans-Rectal Ultrasound of the Female Pelvis for Real-Time MRI-US Fusion Based Needle Tracking โ Durham, North Carolina
Explore by condition: All Uterine Cancer clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.