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Management of Sleep Apnoea Syndrome (SAS) in Patients With Vasovagal Syncope (VVS) — VVS-SAS  

Sleep Apnea Syndromes Clinical Trial

Official title:
Management of Sleep Apnoea Syndrome (SAS) in Patients With Vasovagal Syncope (VVS): a Protocol for the VVS-SAS Registry Study

Clinical Trial Summary

This is a multi-centre, registry-based study whose primary objective is to evaluate the effect of treatment for sleep apnoea syndrome (SAS) on the number of syncope/malaise episodes in a population suffering from both idiopathic, recurrent vasovagal syncope/malaises and SAS.

Clinical Trial Description

Treatment for sleep apnoea syndrome includes continuous positive airway pressure (CPAP) or a mandibular advancement device (MAD). Additional routine follow-up includes 24 hour holter monitoring on a yearly basis, polysomnography on a yearly basis, multiple sleep latency tests, table tilt tests. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04294524
Study type Observational
Source PEAS (Pole d'Exploration des Apnees du Sommeil)
Contact Vincent Puel, MD
Phone +33 557810587
Email vpuel001@gmail.com
Status Recruiting
Phase
Start date February 22, 2017
Completion date February 22, 2022
View Details
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