Clinical trial for deep-cavity wound dressings to evaluate the effectiveness and safety of anti-adhesion after ileostomy
- Conditions
- Diseases of the digestive system
- Registration Number
- KCT0002513
- Lead Sponsor
- Wonbiogen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 68
? Adult male or female over 19 years of age
? Those who are scheduled to undergo reconstruction after reconstruction of the ileum
? Those who are reliable and willing to cooperate in this test, and obey the restrictions for the treatment period
? Pregnant or lactating women, pregnant women with a pregnancy plan
? If you have had laparotomy with incision or have a history of adhesion around the incision site
? Peritoneal infection, intraabdominal infection such as intraabdominal abscess
? Patients who continued to receive Corticosteroids 20 mg / day or more within 30 days before surgery
? If you have blood clotting dysfunction
? If the immune function is decreased
? When researchers evaluate that it is not appropriate to participate in this clinical test
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary efficacy outcome: incidence of adhesions in the pelvic floor area during ileus repair (%)
- Secondary Outcome Measures
Name Time Method Adverse event