Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 3:05 PM
Ignite Modification Date: 2025-12-24 @ 3:05 PM
NCT ID: NCT02792959
Eligibility Criteria: Inclusion Criteria: * Epithelial ovarian carcinoma, fallopian tube, or primary peritoneal carcinoma FIGO IIIC-IV histologically confirmed by biopsy and documented stage and untreated * Pre-treatment abdominopelvic PET-CT and MRI within 4 weeks before neoadjuvant chemotherapy. * During laparoscopy performed by an experienced surgeon in the treatment of ovarian cancer, patient considered ineligible for tumor cell kill at the outset. * A life expectancy of greater than three months * An eligible patient for Paclitaxel and Carboplatine based chemotherapy. * Membership of a social security scheme * Patient information and signed, dated written informed consent Exclusion Criteria: * Pre-treated using chemotherapy, radiology, or surgery for an ovarian cancer. * Contraindication to MRI with the injection of contrast product, i.e, the first three months pregnancy, claustrophobia, major allergic antecedents, pacemaker, some surgery clips, some heart valves, cava filter, implanter pumps, cochlear implants, metallic extraneous malter. * Uncontrolled diabetes * Pregnancy and nursing * Other uncontrolled medical conditions as thyroid pathology, neuropsychiatric disease, infection, coronary insufficiency or grade 3 - 4 heart disease established by association "New York Heart" * Patient deprived of liberty and legally protect adult, or not in position to give consent.
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 18 Years
Study: NCT02792959
Study Brief:
Protocol Section: NCT02792959