Observational Study to Develop a Predictive Score for Adverse Events Post ERCP
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
| Condition(s) | Endoscopic Retrograde Cholangiopancreatography |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| 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. |
| Who can participate | 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 |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | IRCCS Azienda Ospedaliero-Universitaria di Bologna |
| Locations | Bologna, Italy |
| Start date | 2021-03-24 |
| NCT ID | NCT06776874 |
| Official listing | https://clinicaltrials.gov/study/NCT06776874 |