C22.0 C78.7 C25.0 C25.1 C25.2 C25.3 C25.4 C25.9 C25.7 C25.8 C25 C25.9 C22.1 C22.2 C22.3 C22.4 C22.7 C22.9
Conditions
Interventions
Group 1: Intraoperative testing of the automatic placement of the VSI Holomedicine of the manufacturer apoQlar
Sponsors
Pius-Hospital Oldenburg, Universitätsklinik für Viszeralchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with liver- or pancreas diseases, with indication for laparotomic surgery.
Exclusion criteria
Exclusion criteria: No consent to participate in the trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Semiautomatic placement of digital images onto the surgical site | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of usability of the AR-function | — |
Countries
Germany
Contacts
Public ContactVerena Uslar
Carl von Ossietzky Universität Oldenburg
Outcome results
None listed