C25.0
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with histologically proven resectable ductal adenocarcinoma and ability to give written informed consent
Exclusion criteria
Exclusion criteria: Participation in trial interfering with the trial Infiltration of stomach or intestine Pregnancy and breast feeding Risk of incompliance Unwillingness or inability to perform birth control Bilirubin > 2.5 x upper reference value Clinically relevant duodenal stenosis renal insufficiency with GRF<30
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of severe complications within 6 weeks after radiotherapy and surgery | — |
Secondary
| Measure | Time frame |
|---|---|
| 30 day mortality | — |
Countries
Germany
Contacts
Universitätsklinikum FreiburgKlinik für Strahlenheilkunde