A Tailored, Web-Based Self-Management Program to Treat Pain in Chronic Pancreatitis
NCT07223554
Chronic Disease, Chronic Pancreatitis
Ann Arbor, Michigan, United States
View Trial DetailsNCT Number: NCT01321450
Including 150 randomised patient, the studies aim is to determine whether an economisation and/or improvement in terms of operating time, drainage fluid, blood loss, time of hospitalisation can be found using an ultrasonic dissection device versus traditional surgical methods such as stitches an ligations.The study is performed for patients undergoing partial pancreatoduodenectomy.
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Notify Me18 year and older
All sexes
Observational
UH Eppendorf, Hamburg, Germany
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
resectable tumor
Exclusion criteria
palliative resection
Time frame: end of operation
Measurement of time regarding incision-closure-time
Time frame: end of operation
Time frame: within the first 24 hours perioperatively
Time frame: end of hospitalization
Time frame: end of hospitalization
Time frame: within the first 5 days postoperatively
Time frame: end of hospitalization
Postoperative interventions due complications, e.g. pancreatic fistula
Universitätsklinikum Hamburg-Eppendorf
Other
Economisation of Preparation by Using an Ultrasonic Dissection Device in Partial Pancreatoduodenectomy
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