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临床试验/NCT04559867
NCT04559867暂停不适用

Fistulotomy as the Primary Cannulation Technique for All Patients Undergoing ERCP: A Randomized, Controlled Trial

Lawrence Charles Hookey2 个研究点 分布在 1 个国家目标入组 538 人开始时间: 2020年9月10日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
538
试验地点
2
主要终点
Post-ERCP pancreatitis

研究概览

简要总结

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 either making a cut called a needle-knife fistulotomy or a sphincterotomy.

详细描述

The ERCP procedure enables the study doctor to examine regions of the digestive system called the pancreas and bile ducts. After a patient is sedated, 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 into the bile duct (area where bile leaves the liver). X-ray pictures can then be taken to provide further information to the doctor.

During the procedure, 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:

  1. 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.
  2. 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, the doctor determines which cutting technique to use. The decision is entirely up to the individual doctor.

The purpose of this study, called a randomized, controlled trial, is to compare the safety and effectiveness of the two different approaches to the ERCP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients, greater than, or equal to 18 years of age, 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: other benign biliary duct diseases including strictures, primary sclerosing cholangitis and Mirizzi's syndrome requiring biliary decompression. 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,
  • Ability to follow-up in a reliable manner.

排除标准

  • 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),
  • P2Y12 inhibitors not held for 5 days prior to the procedure,
  • Prior biliary sphincterotomy,
  • Concurrent pancreatitis (with inability to tolerate oral intake and requiring pain management),
  • Altered upper GI tract anatomy (e.g. prior gastric bypass surgery such as Roux-en-Y or Billroth 2 gastrojejunostomy),
  • Inability to achieve adequate sedation,
  • Evidence of malignant infiltration of the ampulla or peri-ampullary area,
  • Operator inability to access and identify intra-duodenal portion of the bile duct,
  • Presumptive diagnosis of sphincter of Oddi dysfunction,
  • Inability to access intraduodenal segment due to altered anatomy (eg. ampulla within deep diverticulum),
  • Requirement for pancreatogram or pancreatic intervention,
  • Inability to provide informed consent.

结局指标

主要结局

Post-ERCP pancreatitis

时间窗: Up to 7 days

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

次要结局

  • Cannulation Success Rate(Day 0)
  • Total procedure time(Day 0)
  • Inspection Time(Day 0)
  • Time to successful cannulation(Day 0)
  • Ampullary morphology(Day 0)
  • Difficulty of cannulation(Day 0)
  • Incidence of complications(Up to 7 days)

研究者

发起方
Lawrence Charles Hookey
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Lawrence Charles Hookey

Director, Endoscopy

Queen's University

研究点 (2)

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