Single Use ERCP -SURE Study

Sponsor
Nottingham University Hospitals NHS Trust (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04671095
Collaborator
(none)
50
25

Study Details

Study Description

Brief Summary

We do ERCP procedure (Endoscopic procedure with the help of x-rays) for a variety of reasons such as bile duct stones, bile duct obstruction secondary to bile duct narrowing (Strictures) and for bile leak. The incidence of infection post ERCP is around one in 200. There are some group of patients where this risk is significantly increased. In this high risk group, the risk increases from 1 in 75 to in some diseases 1 in 15 (Described in PIS).

There are some reports that some of the infection may be contributed by contamination of bacteria in the scope. This happens even after diligently sterilizing the scope. A multi-centre study reported that the risk of contamination is as high as 39% but what we do not know is how many resulted in bacterial infection. We do not know what percentage of infection is secondary to the above. The new single use duodenoscope has been introduced in to the market to minimise the risk of post ERCP infection. It is CE marked and a single centre study reported that the above performance of the above scope was comparable to the standard reusable scope. We want to assess the scope simultaneously in multiple different hospitals. In addition, we also want to assess the cost consequence to the NHS for using the above scope. Hence we want to assess the performance of the scope in the high risk groups for infection.

Condition or Disease Intervention/Treatment Phase
  • Device: ERCP procedure with single use duodenoscope

Detailed Description

ERCP is a therapeutic endoscopic procedure done to establish either bile duct or pancreatic duct drainage or both. The indications for ERCP are bile duct stones, bile duct strictures, sphincter of Oddi manometry with sphincterotomy, bile leak, pancreatic duct stones and pancreatic duct stricture. The intended benefits of the procedure are either to relieve bile duct/ pancreatic duct obstruction or facilitate bile duct/ pancreatic duct drainage. It is a minimally invasive procedure and is associated with reduced morbidity compared to surgery.

Gall stones are made of cholesterol, pigment and mixture of cholesterol and pigment. The incidence of stones with in the bile-duct varies from 4.6% to 19%.The stones are predominantly formed in the gall bladder and are displaced from the gall bladder in to the bile duct via the cystic duct. ERCP is an effective and minimally invasive treatment for bile duct stones. Treatment of extra- hepatic biliary strictures; irrespective of their aetiology, is to place a stent across the stricture through ERCP and facilitate biliary drainage.

There is emerging data that the incidence of carbapenem resistant enterobacteriae, Multidrug-resistant Klebsiella pneumoniae, and New Delhi metallo-β-lactamase-producing carbapenem-resistant Escherichia coli (CRE) following exposure to contaminated duodenoscopes (ERCP endoscopes). The main reason for the outbreaks is due to inadequate reprocessing (Cleaning of endoscope post procedure) leading to contamination of endoscpes.

To minimise the risk of contamination and outbreak of above infections, single use disposable duodenoscopes have been brought in to the market. The aim of the study is to assess the performance of the single use duodenoscope against the standard reusable duodenoscope and the cost consequences associated with the above.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prospective Observational Cohort Study: To Assess the Performance of Single Use Duodenoscope
Anticipated Study Start Date :
Jan 18, 2021
Anticipated Primary Completion Date :
Jan 18, 2023
Anticipated Study Completion Date :
Feb 18, 2023

Outcome Measures

Primary Outcome Measures

  1. completion the intended ERCP procedure with single use duodenoscope. [60-120 minutes]

    To assess if the intended ERCP prcodure can be successfully completed with single use disposable duodenoscope.

Secondary Outcome Measures

  1. Rate of complications [30 days post procedure]

    Complications associated with the procedure such as bleeding, pancreatitis, post-ERCP infection and perforation

  2. EQ-5D-5L quality of life questionnaire [30 days]

    Quality of life of patients following procedure (EQ-5D questionnaire)

  3. Endoscopy metrics associated with the procedure [During the procedure]

    1. Time to complete procedure, ease of intubation, ease of intubating duodenum, number of attempts to cannulate CBD

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • • Patients who are at high risk of post ERCP infection such as

  • Jaundice (Bilirubin >21)

  • Primary sclerosing cholangitis

  • Post liver transplant anastomotic stricture

  • Inpatients

  • Combined procedures (Ex: ERCP+ spy glass cholangioscopy)

  • Previous inadequate biliary drainage.

  • Biliary stricture

  • Participant is willing and able to give informed consent for participation in the study.

  • Male or Female, aged 18 years or above.

  • Grade 1-3 ERCP on complexity grading (ASGE grading)

  • Able (in the Investigators opinion) and willing to comply with all study requirements.

  • Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study.

Exclusion Criteria:
  • Patients with CBD stones and no jaundice

  • Sphincter of Oddi manometry.

  • Female participants who is pregnant, lactating or planning pregnancy during the course of the study.

  • Patients who are unable to consent for the study.

  • ERCP for Pancreatic pathology.

  • Grade 4 complex ERCP (ASGE grading)

  • Participant who is terminally ill /ECOG 4

  • Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Nottingham University Hospitals NHS Trust

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nottingham University Hospitals NHS Trust
ClinicalTrials.gov Identifier:
NCT04671095
Other Study ID Numbers:
  • 20GA082
First Posted:
Dec 17, 2020
Last Update Posted:
Dec 21, 2020
Last Verified:
Dec 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Nottingham University Hospitals NHS Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 21, 2020