A cohort study to estimates the preventive effect of the decompression tube
Not Applicable
- Conditions
- Rectal disease undergoing laparoscopic rectal surgery with making diverting ileostomy
- Registration Number
- JPRN-UMIN000038980
- Lead Sponsor
- Minimally Invasive Surgical and Medical Oncology,Fukushima Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1)Patients of rectal cancer with intraoperative peritoneal dissemination or class V diagnosis by ascites cell diagnosis 2)Contaminated and infected surgical cases such as perforation and toxic megacolon 3)Surgery other than laparoscopic surgery such as laparotomy or transsacral surgery 4)Patients required conversion to open surgery or other simultaneous abdominal surgery
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Outlet obstruction incidence from immediately after surgery to closure of Diverting ileostomy
- Secondary Outcome Measures
Name Time Method From postoperative until discharge 1)Number of vomiting 2)Abdominal distention, degree of abdominal pain (evaluated by Numeric Rating Scale (NRS)) 3)Relationship between outlet obstruction and stoma emission