Malignant neoplasm of the whole pancreas (pancreatic head, body, tail, pancreatic duct, endocrine gland portion) and malignant neoplasm of the oesophagus (cervical, thoracic, abdominal) C25 C25.0 C25.1 C25.2 C25.3 C25.4 C15 C15.0 C15.1 C15.2
Conditions
Interventions
Group 1: no intervention/observation group
Study procedure:
Patients are screened for inclusion and exclusion criteria. After inclusion in the study, informed consent is obtained. They then receive
Sponsors
Chirurgische Klinik (Zentrum)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Patients who have undergone pancreatic or esophageal surgery and have a malignant tumor disease is present. The inclusion is independent of tumor status, pre-treatment or surgical procedure. - Patients who have been admitted to a general visceral surgery ward of the Department of Surgery at UKHD as part of their postoperative care and are about to be discharged. - Capable of informed consent. - Sufficient knowledge of the German language, both written and spoken.
Exclusion criteria
Exclusion criteria: Patients in whom the results of the histological examination show that there is no cancerous disease of the pancreas or esophagus. Patients were also excluded if the disease had already progressed to such an extent that only an exploration with sampling could be performed as a surgical procedure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is defined as the evaluation of the experience of patient-centeredness and the patient's experience of it. The stated endpoint corresponds only conditionally to that of a classical endpoint, but seems appropriate in the context of this exploratory study project. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary endpoint is to evaluate the care needs of patients with pancreatic and esophageal cancer in the perioperative setting. The stated endpoint corresponds only conditionally to that of a classical endpoint, but seems appropriate in the context of this exploratory study project. | — |
Countries
Germany
Contacts
Public ContactFranziska Elisabeth Glaß
Chirurgische Klinik (Zentrum)
Outcome results
None listed