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Is Needle Knife Fistulotomy An Effective First Step Strategy For All ERCPs?

Primary Purpose

ERCP, Biliary Disease Tract, Biliary Disease

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Needle knife fistulotomy
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for ERCP focused on measuring Needle Knife Fistulotomy, Sphincterotomy, Post-ERCP pancreatitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients, ages > 18, with an intact sphincter undergoing ERCP by at Kingston Health Sciences Center for therapeutic purposes who can provide informed consent. This includes patients who have confirmed choledocholithiasis on imaging and those who have a high suspicion of it based on imaging and lab values. Patients with and without a high suspicion for cholangitis will be eligible for the study. Other indications include: type 1 sphincter of Oddi dysfunction, gallstone pancreatitis or other benign pancreaticobiliary duct diseases including strictures, primary sclerosing cholangitis and Mirizzi's syndrome. Furthermore, patients with suspected diagnosis of biliary leak following cholecystectomy will also be considered for enrollment in this study.
  2. Ability to read and understand the English language

Exclusion criteria:

  1. Bleeding disorder (Von Willebrand disorder, platelet count <100 000, or INR >1.5)
  2. Therapeutic level anticoagulation with low molecular weight heparin (LMWH), warfarin, or a direct-acting oral anticoagulant (DOAC)
  3. Prior biliary sphincterotomy
  4. Altered upper GI tract anatomy (e.g. prior gastric bypass surgery such as Roux-en-Y or Billroth 2 gastrojejunostomy)
  5. Evidence of Malignant infiltration of the ampulla or peri-ampullary area.
  6. Inability to identify intra-duodenal portion of the bile duct, including deep peri-ampullary diverticulum.

Sites / Locations

  • Kingston Health Sciences Centre

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

All Enrolled Patients

Arm Description

Receive needle knife fistulotomy as a starting technique to gain access to the biliary system

Outcomes

Primary Outcome Measures

Post-ERCP pancreatitis
The primary objective to be examined is the incidence of post-ERCP pancreatitis

Secondary Outcome Measures

Technical success
Determined by successful cannulation of the CBD as evidenced on cholangiogram

Full Information

First Posted
October 4, 2018
Last Updated
January 30, 2020
Sponsor
Queen's University
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1. Study Identification

Unique Protocol Identification Number
NCT03698266
Brief Title
Is Needle Knife Fistulotomy An Effective First Step Strategy For All ERCPs?
Official Title
Is Needle Knife Fistulotomy An Effective First Step Strategy For All ERCPs?
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
November 23, 2018 (Actual)
Primary Completion Date
January 29, 2020 (Actual)
Study Completion Date
January 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Participants in this study will be undergoing a procedure called an endoscopic retrograde cholangiopancreatography (ERCP). This procedure is most commonly performed to help treat conditions affecting specific areas of the digestive system called the pancreas and bile ducts. Patients will consent to allow the study physician to access these areas of the digestive system by making a cut using a technique called a needle-knife fistulotomy. If the physician is unable to gain access through this method, they will make the cut using a technique called a sphincterotomy.
Detailed Description
The ERCP procedure enables doctors to examine the regions of the digestive system called the pancreas and bile ducts. After sedating a patient, a bendable tube with a light (called an endoscope), is inserted through the mouth and into the digestive system. Within the digestive system, the doctor is able to identify the opening to where the gallbladder drains into the small bowel called the ampulla. Using the endoscope, a small plastic tube is then placed in the opening and dye (also called contrast material) is injected bile duct (where bile leaves the liver from). X-ray pictures can then be taken to provide further information to the doctor. Sometimes it is necessary to make a cut to enlarge the opening to allow easier removal of stones from the bile duct or to place plastic tubes (stents) in the bile duct. To make this cut, there are two different approaches that the doctor can take: The standard way of making the cut is referred to as a "sphincterotomy". Using this method, a heated metal wire cuts the opening to the bile duct after a wire has been passed into it. The second way of making the cut is referred to as a "pre-cut". There are various types of "pre-cut" techniques; the technique being evaluated in this study is called the "needle knife fistulotomy". When using this technique, the doctor makes a cut directly into the bile duct using a tiny knife called a "needle knife". Currently, there is not a standard that tells doctors what cutting technique to use. The decision is entirely up to the individual doctor. Patients that participate in this study give their permission to allow the study doctor to use the "needle knife fistulotomy" cutting technique first to gain access to the bile ducts. If the study doctor is unable to gain access through this method, then they will use the standard sphincterotomy technique. The purpose of this study, called a feasibility study, is to determine if the needle-knife fistulotomy is at least as safe and effective as the standard access technique, if not safer. If it can be shown that the needle-knife fistulotomy is safer and/or more effective, then it could change the way that doctors conduct this procedure in Canada and the rest of the world.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ERCP, Biliary Disease Tract, Biliary Disease
Keywords
Needle Knife Fistulotomy, Sphincterotomy, Post-ERCP pancreatitis

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients enrolled in the study will consent to a needle knife fistulotomy as a starting technique to gain access to the biliary system.
Masking
None (Open Label)
Allocation
N/A
Enrollment
84 (Actual)

8. Arms, Groups, and Interventions

Arm Title
All Enrolled Patients
Arm Type
Other
Arm Description
Receive needle knife fistulotomy as a starting technique to gain access to the biliary system
Intervention Type
Procedure
Intervention Name(s)
Needle knife fistulotomy
Intervention Description
A needle knife fistulotomy uses a tiny knife to cut directly into the ampulla to gain access to the biliary system in patients undergoing ERCP
Primary Outcome Measure Information:
Title
Post-ERCP pancreatitis
Description
The primary objective to be examined is the incidence of post-ERCP pancreatitis
Time Frame
Up to 7 days post-procedure
Secondary Outcome Measure Information:
Title
Technical success
Description
Determined by successful cannulation of the CBD as evidenced on cholangiogram
Time Frame
Day of procedure
Other Pre-specified Outcome Measures:
Title
Total procedure time
Description
Measured for completed procedures from the time of esophageal intubation to the time of scope withdrawal from the patient mouth
Time Frame
Day of procedure
Title
Time to successful cannulation
Description
Measured from the time of identification of the papilla to successful CBD cannulation as evident by the cholangiogram
Time Frame
Day of procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients, ages > 18, with an intact sphincter undergoing ERCP by at Kingston Health Sciences Center for therapeutic purposes who can provide informed consent. This includes patients who have confirmed choledocholithiasis on imaging and those who have a high suspicion of it based on imaging and lab values. Patients with and without a high suspicion for cholangitis will be eligible for the study. Other indications include: type 1 sphincter of Oddi dysfunction, gallstone pancreatitis or other benign pancreaticobiliary duct diseases including strictures, primary sclerosing cholangitis and Mirizzi's syndrome. Furthermore, patients with suspected diagnosis of biliary leak following cholecystectomy will also be considered for enrollment in this study. Ability to read and understand the English language Exclusion criteria: Bleeding disorder (Von Willebrand disorder, platelet count <100 000, or INR >1.5) Therapeutic level anticoagulation with low molecular weight heparin (LMWH), warfarin, or a direct-acting oral anticoagulant (DOAC) Prior biliary sphincterotomy Altered upper GI tract anatomy (e.g. prior gastric bypass surgery such as Roux-en-Y or Billroth 2 gastrojejunostomy) Evidence of Malignant infiltration of the ampulla or peri-ampullary area. Inability to identify intra-duodenal portion of the bile duct, including deep peri-ampullary diverticulum.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lawrence C Hookey, MD
Organizational Affiliation
Queen's University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kingston Health Sciences Centre
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 5G2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
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Is Needle Knife Fistulotomy An Effective First Step Strategy For All ERCPs?

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