C15.1 C16.0
Conditions
Interventions
Group 1: Liver function test via LiMAx, FibroScan, blood test, MultiLiverScan, CT, MRI, macroscopy and biopsy
Sponsors
Universitätsklinikum Köln
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: squamous cell carcinoma of the middle or distal esophagus or adenocarcinoma of the esophagogastric junction Typ I or II with a BMI over 30 neoadjuvant radiochemotherapy or chemotherapy Initial staging uT2-3 Nx M0 Informed patients consent
Exclusion criteria
Exclusion criteria: ASA = IV FEV1 < 1,5 l ECOG = 2 Non-resectable primary tumours
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Aim is the comparison of the available non-invasive liver function test with the liver biopsy | — |
Countries
Germany
Contacts
Public ContactDenise Buchner
Universitätsklinikum Köln
Outcome results
None listed