Blood collection: Blood sample is collected during routine blood collection by a medical doctor. No more than 60ml (max.) at one timepoint.
Establishment of a tumor bank, consisting of blood samples of tumor patients and healthy people as controls. The blood samples will be collected systematically together with the corresponding clinical data. The biological samples, the clinical date together with prospective experimental date constitute the entity of the tumor bank.
| Facility | City | Region | Status |
|---|---|---|---|
| Innsbruck Medical University | Innsbruck | Austria | Completed |
| University Hospitals Leuven - Department of Obstetrics and Gynaecology | Leuven | Belgium | Completed |
| Charité University - Campus Virchow Chlinic | Berlin | Germany | Recruiting |
| University Medical Center Freiburg | Freiburg im Breisgau | Germany | Completed |
| University Clinic of Ruhr University Bochum | Herne | Germany | Completed |
| European Institute of Oncology, Division of Gynecologic Oncology, Unit of Preventive Gynecology | Milan | Italy | Withdrawn |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT01763125 on ClinicalTrials.gov ↗ ← All trials in Belgium