C25.0 C24.1 C24.0 C17.0
Conditions
Interventions
Group 1: Control group: conventional dissection with conventional hemostasis (e.g. ligature, suture, clip)
Group 2: Experimental group: Dissection with LigaSure
Sponsors
Klinik für Allgemein-, Viszeral- und Transplantationschirurgie Universitätsklinikum Heidelberg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Older than 18years; clinical suspect for pancreatic head cancer, papilla, distal bile-duct or duodenal carcinoma; operative indication for standard pp-Whipple; written consensus.
Exclusion criteria
Exclusion criteria: Patients that take place in other clinical studies. Restricted mental status and language difficulties.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Operating time (cut/sutural time) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Mortality 2. Intra- and postoperative complications 3. Intraoperative blood loss 4. Hospital stay 5. Hospital re-entry rate (30 days postoperative) 6. Induction and reversal time of anesthesia (anesthesia and operation log) 7. Material consumption perioperative 8. Material costs of the operation 9. Overall costs of the operation 10. Local recrudescence (standard follow-up care) 11. Quality of life (quality of life questionary) | — |
Countries
Germany
Contacts
Public ContactDagmar Anders
Klinisches Studienzentrum der Chirurgie (KSC)
Outcome results
None listed