The International Imaging Registry in Liver Cirrhosis (BAVENO-VI SPSS GROUP).

Summary

The purpose of this study is to perform a multicentre registry of cirrhotic patients who had been submitted to an imagining technique in recent years (angio-CT scan or abdominal MRI), in order to collect anatomical and clinical information. The main objective will be focused on the study of portosystemic shunts and their relation with portal hypertension.

Patient with liver cirrhosis submitted to an abdominal angio-CT scan or a MRI from year 2010 to 2014 will be included in the study. The chosen imaging technique will be angio-CT preferably, but MRI data will also be available. Patients will be identified in every hospital by means of the registry of coded diagnoses and the lists of complementary tests performed. Clinical and radiological data of every patient will be collected. The clinical variables will be obtained from reviewing the patient clinical history. The radiological parameters will be gathered by means of the systematic review of the angio-CT or MRI.

Conditions

• Liver Cirrhosis
• Portal Hypertension
• Hepatic Encephalopathy

Interventions

OTHER

No intervention is studied

Sponsors & Collaborators

• IRCCS Policlinico S. Donato

  collaborator OTHER

• Martin-Luther-Universität Halle-Wittenberg

  collaborator OTHER

• Hospital Clinic of Barcelona

  collaborator OTHER

• Hospital General Universitario Gregorio Marañon

  collaborator OTHER

• Hospital Universitario Ramon y Cajal

  collaborator OTHER

• Odense University Hospital

  collaborator OTHER

• Puerta de Hierro University Hospital

  collaborator OTHER

• Royal Free Hospital NHS Foundation Trust

  collaborator OTHER

• University of Alberta

  collaborator OTHER

• University Hospital, Bonn

  collaborator OTHER

• University Hospital, Gasthuisberg

  collaborator OTHER

• Vienna General Hospital

  collaborator OTHER

• Hospital Universitari Vall d'Hebron Research Institute

  lead OTHER

Principal Investigators

• Joan Genesca, MD · Vall d´Hebron Research Institut. Hospital Vall d´Hebron. Barcelona, Spain.

Eligibility

Min Age

18 Years

Sex

ALL

Healthy Volunteers

No

Timeline & Regulatory

Start

2016-04-30

Primary Completion

2017-10-31

Completion

2017-12-31

Countries

• Spain

Study Locations