Surgey assisting imaging C22.0 C22.1 C22 C22.2 C22.3 C22.4 C22.7 C22.9 C23 C24
Conditions
Interventions
Group 1: The following study procedure is provided:
I. Study inclusion
Information about the aim and procedure of the study
Informed consent for questioning and use of results for scientific purposes
Sponsors
Universitätsklinink für Viszeralchirurgie, Pius-Hospital, Universitätsmedizin Oldenburg
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Patients: informed consent, indication for liver surgery; Surgeons: informed consent
Exclusion criteria
Exclusion criteria: Patients: No consent to participate in the study; Surgeons: No consent to participate in the study; medical students
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison / evaluation of digital image data vs. CT / MRT image data with regard to knowledge / information content and the form of representation | — |
Secondary
| Measure | Time frame |
|---|---|
| In addition, digital image data is projected onto the liver during the operation with AR and checked sonographically regarding anatomical strutures, the position / number of tumors / metastases and tumor infiltration. In addition, a histological validation is carried out. | — |
Countries
Germany
Contacts
Public ContactDaniela Salzmann
Universitätsklinik für ViszeralchirurgieUniversitätsmedizin Oldenburg, Pius-Hospital Oldenburg
Outcome results
None listed