KCT0004239Active, not recruiting未知
Comparison of clinical outcomes after endoscopic submucosal dissection using high versus standard dose proton pump inhibitor : A prospective, randomized controlled trial
Kyung Hee University Hospital0 sites438 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- 未知
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 438
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 19(Year) to o Limit (—)
- Sex
- All
Inclusion Criteria
- •1)Over 19 years old patients who planned to undergo endoscopic submucosal dissection for gastric adenoma or early gastric caner.
- •2) Person who are agreed upon study enrollement.
Exclusion Criteria
- •1)Coagulopathy defined by Prothrombine time > 1.5 INR, activated partial thromboplastin time > 1.5 times above reference value
- •2)Previous history of stomach surgery
- •3)Allergic to PPI (Hypersensitivity or history of hypersensitivity to PPI itself, constituent of PPI or Benzimidazole)
- •4)Pregnant or lactating woman
- •5)If it is impossible to assess one's pain
- •6)Patients using atazanavir or nelfinavir
- •7)Patients using Rilpivirine-containing medication
Investigators
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