IRCCS Azienda Ospedaliero-Universitaria di Bologna
Bologna, 40138, Italy
Location status: Recruiting
Location contact
Francesco Vasuri, MD
CONTACT
Francesco Vasuri, MD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT06729944
The aim of this study is to identify a dysplasia- and CCA-specific NGS panel to increase the diagnostic sensitivity of histological and/or cytological examination of biliary tract stenosis.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Bologna, 40138, Italy
Location status: Recruiting
Francesco Vasuri, MD
CONTACT
Francesco Vasuri, MD
PRINCIPAL_INVESTIGATOR
Patients undergoing biliary tract resection, as part of the normal course of care, at the O.U. General Surgery and Transplantation will be enrolled. Tissue samples will be processed and analysed at the O.U. of Pathological Anatomy.
Clinical, serological and instrumental data from patients, considered necessary for the intended analyses, will be collected for the purposes of the study.
The study will have a total duration of 36 months. It is planned to enrol 50 patients, all belonging to the U.O. Hepatobiliary and Transplant Surgery of the IRCCS Azienda Ospedaliero-Universitaria di Bologna. The size of the population is estimated on the basis of the number of cases/year from the U.O. Hepatobiliary and Transplant Surgery, and is considered sufficient to achieve the primary objective, since it is an exploratory study. Surgical material (resection of biliary tract, possibly hepatectomy or duodenocephalopancreasectomy), which will be sampled according to clinical practice and sent to the O.U. of Pathological Anatomy of the IRCCS AOUBO, where it will be sampled, fixed in formalin, included in paraffin and processed. From paraffin blocks (selected from those obtained from the sampling of surgical pieces according to clinical practice) 2 µm sections will be cut for Next Generation Sequencing investigations.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tissue samples will be processed and analysed at the U.O. of Pathological Anatomy
Time frame: During enrollment period, up to 30 months
Ratio between the number of cases identified with NGS panel and the number of cases identified with standard of care
Contact information is provided by the study sponsor or research team.
Deborah Malvi, MD
CONTACT
Francecso Vasuri, MD
CONTACT
IRCCS Azienda Ospedaliero-Universitaria di Bologna
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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