ASSURE WCD Clinical Evaluation - Detection and Safety Study

NACompletedINTERVENTIONAL
Enrollment

130

Participants

Timeline

Start Date

March 20, 2019

Primary Completion Date

June 18, 2019

Study Completion Date

June 18, 2019

Conditions
Cardiac Arrest, Sudden
Interventions
DEVICE

ASSURE™ Wearable Cardioverter Defibrillator (WCD)

WCD with shock alarms and shock functionality disabled

Trial Locations (10)

20912

Washington Adventist Hospital, Takoma Park

43615

Toledo ProMedica Hospital, Toledo

48109

University of Michigan, Ann Arbor

55905

Mayo Clinic, Rochester

63110

Washington University St Louis, St Louis

70403

Heart Clinic of Hammond, LA, Hammond

98195

University of Washington Medical Center, Seattle

98405

Institute for Research and Innovation MultiCare Health System, Tacoma

99508

Alaska Cardiovascular Research Foundation, Anchorage

08103

Cooper University Health Care, Camden

All Listed Sponsors
collaborator

Regulatory and Clinical Research Institute Inc

OTHER

lead

Kestra Medical Technologies, Inc.

INDUSTRY

NCT03887052 - ASSURE WCD Clinical Evaluation - Detection and Safety Study | Biotech Hunter | Biotech Hunter