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Clinical Trials/KCT0004239
KCT0004239
Active, 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 enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Kyung Hee University Hospital
Enrollment
438
Status
Active, not recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
Kyung Hee University Hospital

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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