Microbiological Assessment of Bile in Patients Undergone to Endoscopic Retrograde Cholangiography (ERCP): the "Microbile Registry"
Launched by AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA · Oct 30, 2023
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
The "Microbile Registry" is a clinical trial that aims to study the types of bacteria present in the bile of patients who are undergoing a procedure called Endoscopic Retrograde Cholangiography (ERCP). This procedure is often used to treat conditions like jaundice, which is a yellowing of the skin and eyes caused by liver or bile duct issues, as well as other biliary diseases. By understanding the microbial environment in the bile, researchers hope to improve treatment options and patient outcomes.
To participate in this study, you must be at least 18 years old and able to give consent. You can join if you have a medical reason for needing an ERCP, whether it is for a benign (non-cancerous) or malignant (cancerous) condition. However, if you have previously had a specific surgery related to the bile ducts, are pregnant or breastfeeding, or cannot provide informed consent, you will not be eligible for this study. If you choose to participate, you can expect to have your bile assessed for bacteria during the ERCP procedure, which could help shape future treatments for similar conditions.
Gender
ALL
Eligibility criteria
- • Main inclusion criteria for patient enrollment were: ability to provide an informed consent; age \>/=18 years; any benignant or malignant ERCP indication.
- All subjects were excluded from the study:
- • Patients who have already undergone endoscopic sphincterotomy
- • Patients unable to express informed consent
- • Pregnant or breastfeeding women
- • Patients with anatomical post-surgical alterations of the upper gastrointestinal (GI) tract
About Azienda Unità Sanitaria Locale Della Romagna
Azienda Unità Sanitaria Locale della Romagna (AUSL Romagna) is a leading public health organization dedicated to providing comprehensive healthcare services in the Romagna region of Italy. As a clinical trial sponsor, AUSL Romagna plays a pivotal role in advancing medical research and innovation by facilitating studies that aim to improve patient outcomes and healthcare delivery. The organization is committed to adhering to the highest ethical standards and regulatory compliance, ensuring the safety and well-being of participants while contributing valuable insights to the scientific community. With a focus on collaboration and community engagement, AUSL Romagna strives to enhance public health through evidence-based practices and groundbreaking clinical research initiatives.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Forlì, , Italy
Forlì, Forlì Cesena, Italy
Patients applied
Trial Officials
Carlo Fabbri, MD
Principal Investigator
AUSL Romagna
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported