CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 39 enrolled
Drug / intervention
Short Term Wearable Defibrillatordevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02188147
NCT02188147N/ACompleted
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Ambulatory Post-Syncope Arrhythmia Protection Feasibility Study Protocol

Zoll Medical Corporation·interventional·Posted Jul 11, 2014·Updated Feb 21, 2023

In Brief

A clinical study evaluating Short Term Wearable Defibrillator for Syncope. Completed, enrolled 39 participants across 6 sites.

Detailed Summary

The purpose of this study is to conduct an observational investigation of a novel care path used to manage emergency department (ED) presenting syncope patients on an outpatient basis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSyncope
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedJul 11, 2014
Enrollment StartAug 1, 2014
Primary CompletionApr 1, 2020
Study CompletionApr 15, 2020
TodayJul 2, 2026
Enrollment to primary: 5.7 yearsPosted 12.0 years ago

Interventions

Short Term Wearable Defibrillatordevice

Short-term Wearable Defibrillator (SWD 1000)