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Clinical Trial Details — Status: Suspended

Administrative data

NCT number NCT02290769
Other study ID # 382 - 072014
Secondary ID
Status Suspended
Phase N/A
First received
Last updated
Start date January 28, 2018
Est. completion date December 14, 2025

Study information

Verified date March 2023
Source Niguarda Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to compare the cannulation time during primary wire guided ERCP (Endoscopic Retrograde Cholangio-Pancreatography) according to two different length of guide wire: long wire or short wire rapid exchange, artery by a prospective randomized trial.


Description:

In primary Endoscopic Retrograde Cholangio-Pancreatography (ERCP) cannulation is wire guided. Up to now there is no doubt about the efficacy of such a procedure. The use of long wire requires the help of another person behind primary operator. The use of short wire rapid exchange allows the primary operator to perform all the steps by himself. Time of cannulation is known to be directly associated to post ERCP pancreatitis. Aim of the study is to assess which length of guide wire allows the shorter cannulation time during primary ERCP. Post ERCP pancreatitis onset will be assessed for all patients


Recruitment information / eligibility

Status Suspended
Enrollment 292
Est. completion date December 14, 2025
Est. primary completion date January 28, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - indication to primary ERCP - ASA (American Society of Anesthesiologists) 1, 2, 3 Exclusion Criteria: - pancreas neoplasia - pancreatitis - ampulloma - duodenum stenosis - under mucous membrane haematoma

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Short guide wire rapid exchange
Use of short guide wire rapid exchange to guide the cannulation during primary ERCP
Long guide wire
Use of long wire to guide the cannulation during primary ERCP

Locations

Country Name City State
Italy Niguarda Hospital Milano

Sponsors (1)

Lead Sponsor Collaborator
Niguarda Hospital

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Time of cannulation Time (in seconds) required to perform a complete and successful deep cannulation of the "biliary papilla" and the biliary tree assessed by timing it and reporting it in the prefashioned database 8 hours from intervention
Secondary Incidence of post ERCP pancreatitis Incidence of post ERCP pancreatitis 8 hours post ERCP
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