Cologne Register of Wearable Defibrillator (CRWD)

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02073942

Enrollment

100

Registered

2014-02-28

Start date

2014-02-28

Completion date

2018-03-31

Last updated

2018-10-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myocardial Infarction, Myocarditis, Ventricular Dysfunction

Brief summary

The wearable cardiac defibrillator (WCD) is an alternative to the implantation of cardioverter defibrillator (ICD) for patients at high risk for sudden cardiac death (mostly bridging therapy). The Cologne register of wearable defibrillator (CRWD) is a prospective register for all patient with an indication of wearable defibrillator.

Interventions

None listed

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Adult patients with an indication for wearable defibrillator

Exclusion criteria

* childs

Design outcomes

Primary

Measure	Time frame
Number of arrhythmic events and arrhythmic risk factors during bridging therapy with wearable defibrillator	3 years

Secondary

Measure	Time frame	Description
Total mortality	1 months and 3 months	Incidence of Treatment-Emergent Adverse Events \[Safety and Tolerability\]

Countries

Germany

Outcome results