Phase 2 Ovarian 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 recurrent primary mucinous ovarian cancer, confirmed through laboratory testing of a tissue or cell sample
- People aged 18 or older
- People who are reasonably able to carry out daily activities (assessed using a standard health scale, confirm with trial site)
- People whose blood counts and organ function meet specific levels when tested within 30 days before registering — including white blood cell counts, platelet counts, and liver and kidney function readings
- People who have had their last chemotherapy or radiation treatment more than 2 weeks before joining (or more than 6 weeks if the treatment was bevacizumab)
- People who are willing and able to sign an informed consent form, either themselves or through a legally authorised representative
Who may not be able to join:
- People who are currently taking part in another experimental treatment trial, or who have received an unapproved experimental treatment within 30 days before the procedure
- People whose mucinous tumour has been confirmed by pathology to have originated from somewhere other than the gynaecological system
- People with known active cancer spread to the brain or central nervous system
- People with a known allergy or sensitivity to cisplatin or any of its ingredients
- People with an uncontrolled illness such as an active infection, unstable heart condition, unmanaged heart rhythm problems, or mental health or personal circumstances that may affect participation
- People who are currently pregnant or breastfeeding
- People with moderate to severe nerve damage in their hands or feet (confirm with trial site)
- People who have previously had an organ or tissue transplant from another person
- People who have previously had a specific type of chemotherapy delivered directly into the abdomen (HIPEC or intraperitoneal chemotherapy)
- People with known large areas of cancer spread outside the abdomen and pelvis
- People with moderate to severe hearing loss or ringing in the ears
Note: People with a history of another cancer may still be considered eligible, depending on whether that cancer or its treatment could affect the safety or results of this trial — the trial site would assess this individually.
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: Aaron Shafer, MD, M.D. Anderson Cancer Center
Phone: 832-885-6133
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
To estimate progression-free survival (PFS) after secondary cytoreductive surgery and HIPEC for women with recurrent primary mucinous ovarian cancer
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.