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Clinical Trials in Italy / NCT06776874
Recruiting Observational

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

NCT06776874 · tracked via the Priya Life Science Italy tracker
Sponsor
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Phase
Observational
Started
2021-03-24
Last updated
2025-01-15

Condition(s) studied

Endoscopic Retrograde Cholangiopancreatography

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \>18 years * Patients admitted with hepato-biliary-pancreatic disease or other pathological conditions that require treatment by ERCP * Obtaining informed consent Exclusion Criteria: * None

Primary outcome measure(s)

  • post-ERCP complications — 14 days
    Identification of independent factors associated with an increased risk of post-ERCP complications.

Trial sites (1)

FacilityCityRegionStatus
IRCCS Azienda Ospedaliero-Universitaria di Bologna Bologna Italy Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06776874 on ClinicalTrials.gov ↗ ← All trials in Italy