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Clinical Trial Summary

Research project in which biological material is sampled and health-related personal data is further used and collected. Coded data are used.


Clinical Trial Description

To collect high quality prospective data on a rare disease in order to elucidate epidemiology, natural history, response to treatment and outcome. In addition, a biobank allows addressing specific scientific issues on a variety of open questions. The cohort will provide a platform for carrying out scientific research projects on AIH. In addition, the cohort will allow collaborations with reference networks on AIH abroad. Measurements and procedures: Enrolment visit and one follow-up visit at least once a year are planned. An additional follow-up visit at 6 months postdiagnosis is planned for newly diagnosed patients. Whole blood is collected for biobanking once a year Optionally, if available and collected during normal clinical procedures, liver fragments are obtained. Number of subjects projected for the entire study (all sites combined): 500 (corresponding to 1/3 of the estimated global AIH population residing in Switzerland, assuming a disease prevalence of 20:100,000) ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03146884
Study type Observational [Patient Registry]
Source Fondazione Epatocentro Ticino
Contact Benedetta Terziroli Beretta-Piccoli, MD
Phone +41919608503
Email benedetta.terziroli@hin.ch
Status Recruiting
Phase
Start date February 16, 2017
Completion date December 31, 2022

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