A Multicenter, single-blind, randomized, parallel-group trial examing the Effectiveness of Precompression during Distal Pancreatectomy.
Not Applicable
- Conditions
- Patients who underwent distal pancreatectomy
- Registration Number
- JPRN-UMIN000042700
- Lead Sponsor
- Hiroshima University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1.patients with severe ischemic heart disease(NYHA > III) 2.patients with grade C liver damage 3.patients required continuous oxygen administration due to severe lung disease 4.patients who received dialysis 5.patients with active cancer disease that may influence perioperative adverse events. 6.Patients who enable to enroll in this trial due to their mental illness. 7.Patients who reject to enroll in this trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of Grade B/C postoperative pancreatic fistula within one month after surgery
- Secondary Outcome Measures
Name Time Method