Endometrial Cancer Trial, Recruiting NCT07631572 Sponsor: Denise Fabian Condition: Endometrial Cancer
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Endometrial Cancer Trial, Recruiting

NCT07631572
Recruiting Not Applicable

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 confirmed by laboratory testing to have a vaginal recurrence of endometrial cancer (specific types: endometrioid adenocarcinoma, uterine serous, carcinosarcoma, or clear cell) or cervical cancer (specific types: squamous, adenosquamous, or adenocarcinoma).
  • People whose vaginal recurrence is suitable for a type of internal radiation treatment called a cesium implant, as determined by the treating doctor.
  • People who have a vaginal tumour that is measurable — at least 1 cm in size on a CT scan, MRI, or by physical measurement if the tumour cannot be seen on imaging.
  • People who previously received external beam radiation to the pelvis for uterine or cervical cancer, provided the previous radiation dose did not exceed safe limits in the treating doctor's judgement.
  • People with a general health and activity level rated 0, 1, or 2 on the Gynecologic Oncology Group performance scale (confirm with trial site for details on what these ratings mean).
  • People who are able to understand the study and are willing to sign a written consent form.

Who may not be able to join:

  • People who currently have, or have been diagnosed with, another active invasive cancer within the last three years — with exceptions for non-melanoma skin cancer, previous cervical cancer in situ, or bladder cancer in situ.
  • People who have evidence of cancer that has spread to distant sites or nearby lymph nodes, visible on imaging at the time of joining the study (people who previously had spread that was treated and is no longer visible on imaging may be considered at the treating radiation oncologist's discretion).
  • People who have received a medication called epoetin alpha (also known as Procrit or Epogen) within one month before the study screening visit.
  • People with a history of allergic reactions to substances chemically or biologically similar to the cesium-131 implant or other agents used in this study.
  • People who are pregnant, as radiation is known to be harmful to a developing baby. People of childbearing potential, and men, are required to use two reliable forms of contraception before, during, and for two months after treatment. Anyone who becomes pregnant or suspects pregnancy during the study must inform their treating doctor immediately.

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 8593232354

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Denise Fabian
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
1 May 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Proportion of participants with organ preservation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov