Prospective intervention study to evaluate safety and effectiveness of newly developed silicon made drain fixing device.
Not Applicable
- Conditions
- Patients who will have surgery in general surgery department.
- Registration Number
- JPRN-UMIN000015844
- Lead Sponsor
- Keio University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients with infection or dermatitis on the drain insertion site. 2) Patients with mental disease who may have risk of self removal of the drain. 3) Patients with diabetes mellitus under insulin therapy, or under dialysis, or patients with immune deficiency. 4) Patients with severe obesity or emaciation. 5) Patients who doctor thinks inappropriate to participate in the study.
Study & Design
- Study Type
- Interventional,observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Safety (complication due to the use of newly developed drain fixing device, troubles with drain such as occlusion) Effectiveness (the pain caused by fixing the drain)
- Secondary Outcome Measures
Name Time Method