C25 C18 C22
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: No age limit Patients with colorectal, pancreatic, hepatocellular and cholangiocellular carcinoma
Exclusion criteria
Exclusion criteria: - muscular disease with disposition for malingant hyperthermia - history of propofol-Infusion syndrome (PRIS) - pregnant women - breast feeding women - no written infomed consent - inability to provide written informed consent - emergency cases - ASA >4
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study endpoint is the size of subcutaneous metastases in a nude mouse model from single cell suspensions from resected tumor specimen. | — |
Secondary
| Measure | Time frame |
|---|---|
| Beta-Cathenin activation in peripheral immune cells (PBMC) and tumor cells. | — |
Countries
Germany
Contacts
Allgemein-, Viszeral- u. Transplantationschirurgie Universitätsmedizin Mainz