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Results of the Tokyo trial of prevention of post-ERCP pancreatitis with risperidone-2: a multicenter, randomized, placebo-controlled, double-blind clinical trial.

Authors :
Uchino R
Isayama H
Tsujino T
Sasahira N
Ito Y
Matsubara S
Takahara N
Arizumi T
Toda N
Mohri D
Togawa O
Yagioka H
Yanagihara Y
Nakajima K
Akiyama D
Hamada T
Miyabayashi K
Mizuno S
Kawakubo K
Kogure H
Sasaki T
Yamamoto N
Nakai Y
Hirano K
Tada M
Koike K
Source :
Gastrointestinal endoscopy [Gastrointest Endosc] 2013 Dec; Vol. 78 (6), pp. 842-850. Date of Electronic Publication: 2013 Jul 30.
Publication Year :
2013

Abstract

Background: Our previous study suggested that a combination of ulinastatin and risperidone reduced post-ERCP pancreatitis (PEP) compared with ulinastatin alone.<br />Objective: The aim of this study was to evaluate the efficacy of risperidone alone for prevention of PEP.<br />Design: A multicenter, randomized, placebo-controlled, double-blind clinical trial.<br />Setting: Two academic hospitals and 5 referral hospitals in Tokyo and Saitama, Japan.<br />Patients: Patients undergoing therapeutic or interventional-diagnostic ERCP.<br />Intervention: The patients were randomized to receive 2 mg of oral risperidone or oral placebo at 0.5 to 2 hours before ERCP.<br />Main Outcome Measurements: The primary endpoint was the incidence of PEP. Secondary endpoints were the incidence of hyperenzymemia and enzyme levels (amylase, pancreatic amylase, lipase). Risk factors for PEP were evaluated.<br />Results: We initially enrolled 500 patients in the study (250 in the risperidone group and 250 in the placebo group), but 17 (11 in the risperidone and 6 in the placebo group) were excluded after randomization. PEP developed in 24 patients (10.0%) in the risperidone group and 21 patients (8.6%) in the placebo group (P = .587). Serum amylase levels at 3 hours after ERCP were lower in the risperidone group (P = .007 in a single test of hypothesis, significance removed by Bonferroni correction for multiple testing). In multivariate analysis, a small papilla of Vater, total procedure time ≥40 minutes, and stenosis of the intrahepatic duct were significantly associated with PEP.<br />Limitations: Multiplicity of study centers and a relatively wide time range of drug administration time.<br />Conclusion: Risperidone did not show a benefit in prevention of PEP in this trial. (<br />Clinical Trial Registration Number: NCT000004592.).<br /> (Copyright © 2013 American Society for Gastrointestinal Endoscopy. Published by Mosby, Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-6779
Volume :
78
Issue :
6
Database :
MEDLINE
Journal :
Gastrointestinal endoscopy
Publication Type :
Academic Journal
Accession number :
23910063
Full Text :
https://doi.org/10.1016/j.gie.2013.06.028