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Percutaneous transhepatic vs. endoscopic retrograde biliary drainage for suspected malignant hilar obstruction: study protocol for a randomized controlled trial

Authors :
Firas Al-Kawas
Harry Aslanian
John Baillie
Filip Banovac
Jonathan M. Buscaglia
James Buxbaum
Amitabh Chak
Bradford Chong
Gregory A. Coté
Peter V. Draganov
Kulwinder Dua
Valerie Durkalski
B. Joseph Elmunzer
Lydia D. Foster
Timothy B. Gardner
Brian S. Geller
Priya Jamidar
Laith H. Jamil
Rajesh N. Keswani
Mouen A. Khashab
Gabriel D. Lang
Ryan Law
David Lichtenstein
Simon K. Lo
Sean McCarthy
Silvio Melo
Daniel Mullady
Jose Nieto
J. Bayne Selby
Vikesh K. Singh
Rebecca L. Spitzer
Brian Strife
Paul Tarnaksy
Jason R. Taylor
Jeffrey Tokar
Andrew Y. Wang
April Williams
Field Willingham
Patrick Yachimski
In alphabetical order for the INTERCPT Study Group and the United States Cooperative for Outcomes Research in Endoscopy (USCORE)
Source :
Trials, Vol 19, Iss 1, Pp 1-6 (2018)
Publication Year :
2018
Publisher :
BMC, 2018.

Abstract

Abstract Background The optimal approach to the drainage of malignant obstruction at the liver hilum remains uncertain. We aim to compare percutaneous transhepatic biliary drainage (PTBD) to endoscopic retrograde cholangiography (ERC) as the first intervention in patients with cholestasis due to suspected malignant hilar obstruction (MHO). Methods The INTERCPT trial is a multi-center, comparative effectiveness, randomized, superiority trial of PTBD vs. ERC for decompression of suspected MHO. One hundred and eighty-four eligible patients across medical centers in the United States, who provide informed consent, will be randomly assigned in 1:1 fashion via a web-based electronic randomization system to either ERC or PTBD as the initial drainage and, if indicated, diagnostic procedure. All subsequent clinical interventions, including crossover to the alternative procedure, will be dictated by treating physicians per usual clinical care. Enrolled subjects will be assessed for successful biliary drainage (primary outcome measure), adequate tissue diagnosis, adverse events, the need for additional procedures, hospitalizations, and oncological outcomes over a 6-month follow-up period. Subjects, treating clinicians and outcome assessors will not be blinded. Discussion The INTERCPT trial is designed to determine whether PTBD or ERC is the better initial approach when managing a patient with suspected MHO, a common clinical dilemma that has never been investigated in a randomized trial. Trial registration ClinicalTrials.gov, Identifier: NCT03172832. Registered on 1 June 2017.

Details

Language :
English
ISSN :
17456215
Volume :
19
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.f827d93154b4a15acb6862ef0de3369
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-018-2473-2