visceral or vascular surgery
Conditions
Interventions
Group 1: Included are patients planned for visceral or vascular surgery. By participating in the study, patients do not undergo any additional examinations
in particular, no additional imaging examinations with radiation exposure are performed. The choice of the surgical procedure is independent of the study at hand and depends on the assessment of the s
Sponsors
Universitätskrankenhaus Carl Gustav Carus DresdenKlinik und Poliklinik für Viszeral-, Thorax- und Gefäßchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Indication for visceral and/or vascular surgery - Surgery using the OR1® system or surgery in a hybrid OR using the Artis pheno® angiography system - available pre- and intraoperative imaging - signed consent form
Exclusion criteria
Exclusion criteria: - speech problems or impaired mental state - missing compliance - Known epilepsy of the surgical staff when using HTC Vive® data glasses - surgical medical staff as carriers of implanted electronic medical devices such as pacemakers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main objective is the acquisition, analysis and integration of image and sensor data, and their use for research projects in surgical robotics, augmented and virtual reality, and the development of cognitive surgical assistance systems. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Preoperative imaging information - Intraoperative complication rate and type - type of surgery, - duration - Postoperative tumor status, localization and Histology | — |
Countries
Germany
Contacts
Public ContactMarius Distler
Universitätskrankenhaus Carl Gustav Carus DresdenKlinik und Poliklinik für Viszeral-, Thorax- und Gefäßchirurgie
Outcome results
None listed