D13.6
Conditions
Interventions
Group 1: Observational study: All IPMN patient receive treatment in accordance with guidelines depending on their clinical presentation - conservatively for side duct IPMN, operatively for main duct I
Sponsors
Universitätsklinikum Hamburg-Eppendorf
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: IPMN diagnosis; written consent
Exclusion criteria
Exclusion criteria: no written consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Establishment of a liquid biopsy protocol to achieve a detailed molecular characterisation of IPMN and allow risk stratification of malignancy. | — |
Secondary
| Measure | Time frame |
|---|---|
| We aim to analyse blood samples from 50 konservatively and 50 operatively treated IPMN patients and correlate the results of circulating epithelial cells and cell-free DNA with existing KRAS and GNAS mutations and the risk of malignancy. | — |
Countries
Germany
Contacts
Public ContactChristine Nitschke
Klinik für Allgemein-, Viszeral- und ThoraxchirurgieUniversitätsklinikum Hamburg-Eppendorf
Outcome results
None listed