JPRN-jRCT1041200056
Recruiting
未知
Randomized controlled trial of surgical wounds antisepsis with aqueous povidone-iodine for prophylaxis of surgical site infection in gastroenterological surgery. - SURPRISE trial
Takeuchi Hiroya0 sites700 target enrollmentOctober 28, 2020
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Takeuchi Hiroya
- Enrollment
- 700
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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