Ovarian Cancer Trial, Recruiting NCT04291612 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Ovarian Cancer
Back to Ovarian Cancer

Ovarian Cancer Trial, Recruiting

NCT04291612
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:

  • You are at least 18 years old
  • You are generally healthy and able to carry out most daily activities (confirm with trial site regarding fitness level assessment)
  • You have been diagnosed with a specific type of uterine cancer called endometrioid adenocarcinoma, confirmed by a biopsy or a procedure to sample the uterine lining
  • Scans and physical examination show the cancer appears to be contained within the uterus, with no signs of spread to other areas, lymph nodes, or the cervix
  • You are considered healthy enough to have surgery
  • Your planned surgery includes removal of the uterus (hysterectomy), removal of the ovaries and fallopian tubes on both sides, and a procedure to check specific nearby lymph nodes (sentinel lymph node biopsy)
  • You have not had another cancer (other than certain common skin cancers) in the past 5 years
  • You have not had chemotherapy or radiation therapy for uterine cancer before
  • You have not had any previous radiation treatment to your pelvis or abdomen
  • You have read and signed a form agreeing to take part in the trial
  • After surgery, your final pathology report confirms the cancer is a Stage I intermediate-risk endometrioid cancer and is still confined to the uterus (confirm exact staging details with trial site)
  • After surgery, the sentinel lymph nodes that were tested came back negative (no cancer found in those lymph nodes)
  • The fluid tested from inside your abdomen during surgery showed no cancer cells
  • After surgery, your medical team recommends either no further treatment or radiation treatment directed only to the vaginal area

Who may not be able to join:

  • Scans or physical examination suggest the cancer has spread beyond the uterus, to lymph nodes, or to the cervix before surgery
  • There is a medical reason why the sentinel lymph node mapping procedure cannot be done
  • Your planned treatment does not include surgery, or the surgery does not include removal of the uterus, both ovaries and fallopian tubes, and the sentinel lymph node procedure
  • During surgery, cancer is found outside the uterus or in the lymph nodes
  • Any cancer cells — even very small amounts — are found in the pelvic lymph nodes after surgery
  • The uterus is not removed during surgery
  • Both ovaries and fallopian tubes are not removed (unless one side had already been removed before this trial)
  • The sentinel lymph node mapping procedure does not work on one or both sides
  • A full removal of all pelvic lymph nodes is carried out during surgery
  • A more extensive type of hysterectomy (called a radical type C hysterectomy) is performed
  • The final pathology report shows the earliest stage and lowest-grade form of this cancer (Stage IA, Grade 1 or 2, with less than half of the uterine wall affected)
  • The final pathology report shows a more advanced form (Stage IB, Grade 3)
  • The final pathology report shows a different type of uterine cancer (such as serous, clear cell, or other specific types) rather than endometrioid
  • The lymph node samples collected during surgery come back empty (no lymph node tissue found to test)
  • Cancer cells are found in the abdominal fluid tested during surgery

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 20 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: Nadeem Abu-Rustum, MD, Memorial Sloan Kettering Cancer Center

Phone: 212-639-7051

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
Registry
ClinicalTrials.gov
Start date
26 February 2020
Est. completion
26 February 2027

Where this trial is recruiting

🇨🇿 Czechia 🇮🇹 Italy 🇳🇴 Norway 🇺🇸 United States

Primary endpoints

Incidence of pelvic/non-vaginal recurrence at 36 months

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: 20 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