Randomized controlled trial of surgical wounds antisepsis with aqueous povidone-iodine.
- Conditions
- Gastroentelogical surgery
- Registration Number
- JPRN-jRCT1041200056
- Lead Sponsor
- Takeuchi Hiroya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 700
Intended for patients who meet all of the following criteria:
1. Patients who are over 20 years old when obtaining consent (regardless of gender)
2. Patients undergoing gastroentelogical surgery (such as surgery for esophagus, stomach, small intestine, large intestine, liver, biliary tract, or pancreas) meeting wound class 2, 3, 4) .
3. Patients who have received sufficient explanation for participation in this study, and who have provided written consent.
Patients who violate any of the following will not be included in this study:
1) Patients who have allergy for popidone iodine.
2) follow-up failure due to pass away or other reasons
3) Patients who hav active infection excluding viral hepatitis
4) Patients who are in pregnancy or may be pregnant.
5) Patients lactating.
6) Patients with sever thyroid dysfunction.
7) Any patients who judged to be inappropriate by the study investigators.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method