C25
Conditions
Interventions
Group 1: Observational trial:
The blood draw takes place during routine blood draws perioperatively and during follow-up. No additional portal vein punctures are necessary, as blood is taken from rese
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: consent, PDAC, resectable
Exclusion criteria
Exclusion criteria: no consent, other than PDAC, not resectable
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The overall aim of the study is to establish liquid biopsy protocols for PDAC patients in order to enable a more detailed molecular characterization of the disease and performance of functional test such as drug testing on the cells in the future. | — |
Secondary
| Measure | Time frame |
|---|---|
| KRAS Hot spot Mutation analysis, 24months follow up, WGS of single cells, cfDNA quantities, CTC counts, portal vein vs. peripheral vein | — |
Countries
Germany
Contacts
Public ContactChristine Nitschke
Klinik für Allgemein-, Viszeral- und Thoraxchirurgie; Universitätsklinikum Hamburg-Eppendorf
Outcome results
None listed