PredERCP: Prediction of PEP Based on the Appearance of the Major Duodenal Papilla

Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05800626
Collaborator
(none)
1,740
1
33
52.7

Study Details

Study Description

Brief Summary

This observational, prospective study aims at evaluating how the occurrence of post-Endoscopic Retrograde CholangioPancreatography (ERCP) acute pancreatitis (PEP) could be influenced by difficult biliary cannulation that might be previously assessed by the morphological appearance of native major papilla in all the patients undergoing ERCP.

The rate of successful biliary cannulation across papilla types could be used as intraprocedural quality and competence metrics during training. Moreover, recognizing difficult papillae could allow reserving those to experts to decrease the odds of failed cannulation.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endoscopic Retrograde Cholangio-Pancreatography (ERCP)

Study Design

Study Type:
Observational
Anticipated Enrollment :
1740 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prediction of Post-Endoscopic Retrograde Cholangio-Pancreatography Pancreatitis Based on the Appearance of the Major Duodenal Papilla: a Prospective, Observational, Cohort Study
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2025
Anticipated Study Completion Date :
Dec 31, 2025

Outcome Measures

Primary Outcome Measures

  1. Rate of PEP occurrence distributed between the different native major duodenal papilla types [within 48 hours after the procedure]

Secondary Outcome Measures

  1. Rate of difficult biliary cannulation (> 5 cannulation attempts and/or > 5 minutes attempting to cannulate biliary duct and/or at least one passage in the pancreatic duct) distributed between the different native major duodenal papilla types [during the procedure]

  2. Rate of difficult biliary cannulation distributed between the different types of the intramural papillary segments on fluoroscopic images [during the procedure]

  3. Rate of intraoperative complications distributed between the different native major duodenal papilla types [during the procedure]

  4. Rate of postoperative complications except for PEP (up to 48 hours after ERCP) distributed between the different native major duodenal papilla types [within 48 hours after the procedure]

  5. Difference in the rate of difficult biliary cannulation between ERCP experts (>300 performed procedures) and fellows (<300 performed procedures) [during the procedure]

  6. To evaluate the occurrence of intra- and post-procedural complications but PEP, fluoroscopic morphology of the papillary segment of distal bile duct, perioperative and intraoperative risk factors [within 48 hours after the procedure]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with native duodenal papilla;

  • Any indication to ERCP +/- biliary sphincterotomy of duodenal major papilla;

  • Patients able to provide a written informed consent

Exclusion Criteria:
  • ERCP performed for disorders unrelated to biliary tract;

  • Previous upper gastrointestinal tract surgery;

  • Presence of a duodenal stricture (either malignant or benign);

  • Presence of a malignant infiltration of the papilla;

  • Concomitant anticoagulant and/or P2Y12 inhibitors therapy (clopidogrel, prasugrel, ticagrelor) that precludes the treatment;

  • INR > 1.5;

  • Platelets count < 80000/mm3;

  • Unwillingness to sign written informed consent.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy 00168

Sponsors and Collaborators

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
ClinicalTrials.gov Identifier:
NCT05800626
Other Study ID Numbers:
  • 5534
First Posted:
Apr 5, 2023
Last Update Posted:
Apr 5, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 5, 2023