Phase 2 Endometrial Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with complex atypical endometrial hyperplasia (an abnormal thickening of the uterine lining) or early-stage (grade 1) uterine cancer, confirmed by a tissue biopsy — including those already receiving hormone treatment (progestin) to manage this condition without surgery
- People who have not yet gone through menopause and still have a uterus
- People whose general health and ability to carry out daily activities falls within an acceptable range, as assessed by their doctor (confirm with trial site)
- People aged 18 to 45 years old
- People who are choosing to keep their uterus rather than have it removed — for example, to preserve fertility or for other personal or medical reasons
- People with a body mass index (BMI) of 30 or higher (which falls in the category considered medically obese)
- People who are willing to have a hormonal intrauterine device (IUD) inserted as part of the study, even if they have previously or are currently using progestin hormone treatment
- People who are able to understand the study information and are willing to sign a consent form
Who may not be able to join:
- People currently receiving chemotherapy or radiation therapy for any type of cancer
- People who are pregnant or breastfeeding, or who cannot confirm a negative pregnancy test during the screening period and within 7 days before the IUD is placed
- People who have an active pelvic infection at the time of IUD placement, or who have another medical reason that makes IUD placement unsuitable in their doctor's opinion
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Andrea R Hagemann, M.D., MSCI, Washington University School of Medicine
Phone: 314-362-1763
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Number of participants with atypical endometrial hyperplasia (AEH)-free biopsy
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.