Actively Recruiting

Age: 18Years +
FEMALE
NCT07062016

Molecular and ctDNA Characterization of High-Risk Endometrial Cancer

Led by Mayo Clinic · Updated on 2026-04-13

100

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study seeks to better understand the recurrence of high-risk endometrial cancer. It will collect information about cancer genetics to find out various hereditary or cancer specific genetic variants that may have a role in diagnosis or management and prognosis of cancer. It also seeks to develop a genetic results and medical record databank for future studies.

CONDITIONS

Official Title

Molecular and ctDNA Characterization of High-Risk Endometrial Cancer

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Planned complete surgical staging at Mayo Clinic including total hysterectomy, bilateral salpingo-oophorectomy, and lymph node assessment (sentinel node mapping allowed)
  • At least one preoperative or postoperative aggressive disease feature as defined by FIGO staging
  • Preoperative biopsy showing grade 3 endometrioid or non-endometrioid endometrial cancer
  • Preoperative grade 1-2 endometrioid cancer with evidence of extrauterine disease on imaging (CT, MRI, or PET)
  • Postoperative endometrial cancer with risk factors such as non-endometrioid histology, grade 3, lymphovascular space invasion, deep myometrial invasion, isolated tumor cells in sentinel lymph node, or stage II to IV disease
  • Willing to provide written informed consent
  • Willing to provide mandatory blood and tissue specimens for research
  • Willing to return for clinical follow-up
Not Eligible

You will not qualify if you...

  • Receiving or have received neoadjuvant chemotherapy
  • Pregnant before surgery

AI-Screening

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Trial Site Locations

Total: 1 location

1

Mayo Clinic in Rochester

Rochester, Minnesota, United States, 55905

Actively Recruiting

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Research Team

C

Clinical Trials Referral Office

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

1

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