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Recruiting NCT06776874

NCT06776874 Observational Study to Develop a Predictive Score for Adverse Events Post ERCP

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Clinical Trial Summary
NCT ID NCT06776874
Status Recruiting
Phase
Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Condition Endoscopic Retrograde Cholangiopancreatography
Study Type OBSERVATIONAL
Enrollment 981 participants
Start Date 2021-03-24
Primary Completion 2025-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 981 participants in total. It began in 2021-03-24 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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 Criteria

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

Contact & Investigator

Central Contact

Lorenzo Fuccio, MD

✉ lorenzo.fuccio@aosp.bo.it

📞 0512143338

Principal Investigator

Lorenzo Lorenzo, MD

PRINCIPAL INVESTIGATOR

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Frequently Asked Questions

Who can join the NCT06776874 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Endoscopic Retrograde Cholangiopancreatography. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06776874 currently recruiting?

Yes, NCT06776874 is actively recruiting participants. Contact the research team at lorenzo.fuccio@aosp.bo.it for enrollment information.

Where is the NCT06776874 trial being conducted?

This trial is being conducted at Bologna, Italy.

Who is sponsoring the NCT06776874 clinical trial?

NCT06776874 is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The principal investigator is Lorenzo Lorenzo, MD at IRCCS Azienda Ospedaliero-Universitaria di Bologna. The trial plans to enroll 981 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology