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 @ 4:26 PM
Ignite Modification Date: 2025-12-24 @ 4:26 PM
NCT ID: NCT00290966
Eligibility Criteria: Inclusion Criteria: * Patient's consent form obtained, signed and dated before beginning specific protocol procedures. * Gastric adenocarcinoma including adenocarcinoma of the esophagogastric junction, histologically proven. * Measurable and/or evaluable metastatic disease; if a single metastatic lesion is the only manifestation of the disease, cytology or histology is mandatory. Locally recurrent disease is accepted provided that there is at least one measurable lesion (e.g. lymph node). * Performance status Karnofsky index \> 70%. * Life expectancy of more than 3 months. * Adequate haematological and biochemistry parameters * No prior palliative chemotherapy, previous adjuvant (and/or neo-adjuvant) chemotherapy is allowed if more than 12 months has elapsed between the end of adjuvant (or neo-adjuvant) therapy and first relapse. Exclusion Criteria: * Pregnant or lactating women. * Patients (M/F) with reproductive potential not implementing adequate contraceptive measures. * Other tumor type than adenocarcinoma (leiomyosarcoma ; lymphoma). * Any prior palliative chemotherapy. Prior adjuvant (and/or neo-adjuvant) chemotherapy with a first relapse within 12 months from the end of adjuvant (or neo-adjuvant). * Prior treatment with taxanes. Prior CDDP as adjuvant (and/or neo-adjuvant) chemotherapy with cumulative dose \> 300 mg/m².
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 75 Years
Study: NCT00290966
Study Brief:
Protocol Section: NCT00290966