Observational Study to Develop a Predictive Score for Adverse Events Post ERCP

Recruiting now

Conditions studied: Endoscopic Retrograde Cholangiopancreatography

In brief

The main objective of the study is: the identification of independent factors associated with an increased risk of post-ERCP complications. Other objectives are: the development of a predictive model of events post-ERCP adverse events and its validation; geographic validation of a predictive model already published in the literature using data collected during the study and the evaluation of the rate of post-ERCP AEs in the centers involved in the study.

Key facts

Study ID

NCT06776874

Run by

IRCCS Azienda Ospedaliero-Universitaria di Bologna

People needed

981

Starts

2021-03-24

Expected to finish

2025-12-31

Last updated by the study team

2025-01-15

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age >18 years
• Patients admitted with hepato-biliary-pancreatic disease or other pathological conditions that require treatment by ERCP
• Obtaining informed consent

You may not qualify if…

• None

Where it is running

• IRCCS Azienda Ospedaliero-Universitaria di Bologna — Bologna, Italy (enrolling)

Full record on ClinicalTrials.gov

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