The AVIS Study is a retrospective multicenter international study that aims to answer a series of questions on the use and performance of adrenal venous catheterization (AVS) for the diagnosis of primary hyperaldosteronism subtype. A questionnaire will be circulated among the centres that are internationally recognized and have published in the field of AVS and have agreed to participate in the study.
Clinical Study
Summary
Study Name: Adrenal Vein Sampling International Study (AVIS Study)
Status: Completed
Conditions: Primary aldosteronism
Interventions: Observational only
Locations: Hospital of The University of Pennsylvania, Philadelphia, Philadelphia, Pennsylvania, United States, UT Southwestern Medical Center, Dallas, Texas, United States, Medical College of Wisconsin, Menomonee Falls, Wisconsin, United States; Endocrine Hypertension Research Centre, University of Queensland School of Medicine, Greenslopes Hospital, Brisbane, Australia; Foothills Medical Centre, University of Calgary, Calgary, Alberta, Canada, Centre Hospitalier de l’Universite de Montreal (CHUM), Montreal, Quebec, Canada; General Faculty Hospital, Prague, Prague, Czech Republic, University of Paris, Hôpital Europa en Georges Pompidou, Paris, France; Christian J Strasburger, Berlin, Germany, Heinrich Heine University Dusseldorf, Dusseldorf, Germany, Medizinische Klinik Innenstadt, Munich, Germany, University Hospital Wuerzburg, Wuerzburg, Germany, Dept Clinical and Experimental Medicine (DMCS), University Hospital of Padova, Italy, Padua, Italy, Medicina 2, Dipartimento di Medicina Interna e Specialità Mediche, Azienda Ospedaliera Santa Maria Nuova, Reggio Emilia, Italy; National Hospital Organization, Kyoto Medical Center, Kyoto, Japan|Tohoku University Hospital, Sendai, Japan; Institute of Clinical Endocrinology, Tokyo Women’s Medical University, Tokyo, Japan; Yokohama Rosai Hospital, Yokohama City, Japan, Radboud University Nijmegen Medical Center, Nijmegen, Netherlands, National Taiwan University Hospital, Taipei, Taiwan
Study link: https://ClinicalTrials.gov/show/NCT01234220
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