KCT0008240Not yet recruiting未知
ecessity and effectiveness of empirical antibiotic use in mild to moderate acute inflammatory gallbladder disease; a Multicenter double-blind, randomized, placebo-controlled trial
The Catholic University of Korea, Seoul St. Mary's Hospital0 sites370 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Enrollment
- 370
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 19(Year) to 69(Year) (—)
- Sex
- All
Inclusion Criteria
- •? Patients who are scheduled to undergo laparoscopic surgery among patients with acute cholecystitis who have no evidence of systemic infection between the ages of 19 and 70
- •? Patients with acute cholecystitis with preserved gallbladder walls in the group of patients with acute cholecystitis (grade I by Tokyo guidelines) and moderate (grade II)
- •? Cholecystitis with gallbladder wall thickness of more than 4mm or adhesion to surrounding organs due to gallbladder inflammation
- •? A person who voluntarily signs a written consent form after hearing and understanding the description of this clinical trial
Exclusion Criteria
- •? Those who are scheduled to undergo elective gallbladder surgery (chronic cholecystitis, etc.)
- •? gallbladder disease, not inflammatory disease (GB Cancer, GB polyp)
- •? Among the patients with acute cholecystitis, patients with grade II or III by Tokyo guidelines with unpreserved gallbladder walls
- •? Pregnant or lactating women
- •? A person who performs surgery simultaneously due to other organ diseases.
- •? Those with immunosuppressive and hemorrhagic tendencies
- •? A person who performed percutaneous cholecyst drainage (PTGBD) before alcohol
- •? A person who is required to install a drainage tube during surgery
- •? People who overreact to cephalosporin antibiotics.
- •? A person who participates in another clinical trial within 3 months prior to screening
- •? Other persons deemed unfit for participation in this clinical trial by the tester;
Investigators
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