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Clinical Trial Summary

The purpose of the study is to compare the positivity rate associated with a novel simplified Tilt-Table (TT) test protocol versus the conventional TT protocol


Clinical Trial Description

All patients with unexplained syncope at initial evaluation with indication to perform a Head up tilt test (HUTT) will be randomized to "conventional" HUTT protocol or "fast" HUTT protocol characterized by a stabilization phase of 5 min in the supine position; a passive phase of 10 min at a tilt angle of 60 degrees; a provocation phase of further 10 min after 300 micrograms NTG sublingual spray. The novel simplified "fast" HUTT protocol has been designed to provide non inferior positivity rates as compared with the conventional protocol in the selected population. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05029323
Study type Interventional
Source University of Campania "Luigi Vanvitelli"
Contact Vincenzo Russo, MD PhD
Phone +390817062355
Email vincenzo.russo@unicampania.it
Status Recruiting
Phase N/A
Start date January 7, 2020
Completion date January 7, 2023

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