Robotic interventions due to different underlying diseases
Conditions
Interventions
Group 1: Robot-assisted interventions in general and visceral surgery and urology
Sponsors
Universitätsklinikum Ulm
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: • Planned robot-assisted procedure • Age = 18 years • Consent to participate in the study by written informed consent after prior detailed information about the study
Exclusion criteria
Exclusion criteria: • Contraindications to minimally invasive or robot-assisted surgery • Language or comprehension problems • Expected non-compliance
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is a prospective database. There is no dedicated primary endpoint here. A primary end point is defined for specific projects that are processed using the database. | — |
Secondary
| Measure | Time frame |
|---|---|
| Procedure-specific target variables: 1. Type of procedure 2. Upgrade time 3. Docking time 4. Console time 5. Duration of the operation 6. Intraoperative blood loss Complication-specific outcomes: 1. Postoperative in-hospital and 30-day mortality 2. Superficial and deep Surgical site infection according to CDC 3. Reoperation rate within 90 days. 4. Reintervention rate (e.g. interventional drainage) 5. Rate of organ-space infections according to CDC Organ-specific complications depending on the type of intervention (“core outcome sets”) with patient-reported outcomes 1.) Pancreas 2.) Colorectum 3.) Stomach and upper GI tract 4. Liver 5.) Prostate 6.) kidney Recovery-specific outcomes: 1.) Duration of the postoperative hospital stay in days 2.) Rate of re-hospitalization within 90 days 3.) Regaining the ability to work or complete everyday ability In the case of oncological indications, pathological outcomes: TNM, R status. | — |
Countries
Germany
Contacts
Public ContactFelix Hüttner
Universitätsklinikum UlmKlinik für Allgemein- und Viszeralchirurgie
Outcome results
None listed