CT-guided percutaneous biopsy of the liver
Conditions
Interventions
Group 1: Percutaneous biopsy with the AR system
Group 2: Percutaneous biopsy with CT-fluoroscopy
Sponsors
Universitätslinik für Radiologie und Nuklearmedizin Magdeburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -patients with CT-assisted transcutaneous punctures of the liver, with indication for liver biopsy -written informed consent of the study participant
Exclusion criteria
Exclusion criteria: -patients under the age of 18 -pregnant patients -contraindications for sonography or CT imaging, or biopsies performed with these procedures -uncontrollable intolerance to contrast agent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -comparison of radiation exposure of patient and staff, based on the dose values output by the CT. | — |
Secondary
| Measure | Time frame |
|---|---|
| -comparison of the intervention time (incision to suture time) -Comparison of the set-up time (door to incision time) -comparison of complications, evaluation according to the CTCAE-classification for surgical and medical procedures | — |
Countries
Germany
Contacts
Public ContactKarl Rohmer
Universitätslinik für Radiologie und Nuklearmedizin Magdeburg
Outcome results
None listed