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: 2025-12-25 @ 5:03 AM
Ignite Modification Date: 2025-12-25 @ 5:03 AM
NCT ID: NCT00712218
Eligibility Criteria: Inclusion Criteria: * Primary diagnosis of invasive epithelial ovarian cancer FIGO stage IIB-IV (IV only if resectable metastasis in pleura, liver, spleen, and/or abdominal wall) * Macroscopic complete resection * Age: 18 - 75 years * Patients who have given their signed and written informed consent * Good performance status (ECOG 0/1) Exclusion Criteria: * Non epithelial ovarian malignancies and borderline tumors * Intraoperative clinically suspicious lymph nodes (bulky nodes) * Secondary invasive neoplasms in the last 5 years (except synchronal endometrial carcinoma FIGO IA G1/2, non melanoma skin cancer, breast cancer T1 N0 M0 G1/2) or with any signs of relapse or activity. * Recurrent ovarian cancer * Prior chemotherapy for ovarian cancer or abdominal/pelvic radiotherapy * Diseases of the lymph system (including lymph edema of unknown origin) * Clinical relevant dysfunctions of blood clotting (including medicamentous conditioned reasons, e.g. ASS, if not stopped at least 7 days prior to surgery) * Any significant medical reasons, age or performance status that will not allow to perform the study procedures (estimation of investigator) * Prior retroperitoneal lymph node dissection (systematic or sampling) * Pregnancy * Dementia or significantly altered mental status that would prohibit the understanding and giving of informed consent * Any reasons interfering with regular follow-up
Healthy Volunteers: False
Sex: FEMALE
Minimum Age: 18 Years
Maximum Age: 75 Years
Study: NCT00712218
Study Brief:
Protocol Section: NCT00712218