Endometrial Cancer Trial, Recruiting NCT05421650 Sponsor: CHA University Condition: Endometrial Cancer
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Endometrial Cancer Trial, Recruiting

NCT05421650
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:

  • Women between 20 and 70 years of age
  • People newly diagnosed with a specific type of cervical cancer — either squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma
  • People whose scans (CT or MRI, sometimes PET-CT) show enlarged lymph nodes in the pelvis or near the major abdominal blood vessels, meeting specific size measurements (confirm with trial site for exact details)
  • People for whom doctors have planned a treatment combining chemotherapy and radiation therapy for cervical cancer
  • People with a general health and activity level rated as 0 or 1 on a standard medical scale, meaning largely able to carry out daily activities without restriction
  • People who have given written consent to take part in the study
  • People for whom imaging scans have confirmed that surgery to remove affected lymph nodes would be possible

Who may not be able to join:

  • People diagnosed with any other cancer (apart from thyroid cancer, and excluding very early-stage cancers) within the past 5 years
  • People who are pregnant or plan to become pregnant during the study period
  • People with an active infection or a severe ongoing inflammation that cannot be treated
  • People whose health condition means doctors have determined surgery would not be safe for them
  • People whose health condition means doctors have determined chemotherapy would not be safe for them
  • People who have previously received radiation therapy to the pelvic area
  • People who have previously had a partial (subtotal) hysterectomy
  • People whose cancer has spread to distant areas of the body beyond the pelvic or abdominal lymph nodes — for example, to the lungs, or to lymph nodes near the collarbone or groin

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 22 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

Principal Investigator: Ju-Won Roh, CHA University Ilsan Medical Center

Phone: +82-31-782-8312

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
CHA University
Registry
ClinicalTrials.gov
Start date
1 August 2022
Est. completion
31 December 2030

Where this trial is recruiting

🇮🇳 India 🇮🇹 Italy 🇷🇴 Romania 🇰🇷 South Korea 🇻🇳 Vietnam

Primary endpoints

PFS

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: 22 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