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Study identifier: NCT07324031 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Parasternal Extravascular ICD System Pivotal Clinical Investigation (ALARION EV) Study

Condition: Ventricular Arrythmia · Ventricular Fibrillation · Ventricular Tachycardia  ·  Sponsor: AtaCor Medical, Inc.

PhaseNA
Planned participants280
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The ALARION EV Study is a prospective, multi-center, single-arm, non-randomized study without concurrent or historical controls. The purpose of this pivotal study is to generate evidence of safety and effectiveness to apply for regulatory approvals for commercialization of the Parasternal EV-ICD System. The objective of the study is to demonstrate safety and effectiveness of the Parasternal EV-ICD System through 6-months.

This description comes directly from the study's public registry record.

Talk to the study team

Sarah Hase, BS, CCRA  ·  +1 949-545-9820  ·  sarah@atacor.com

Always discuss trial participation with your own doctor first.

Locations (35)

Honor HealthScottsdale, Arizona, United StatesNot Yet Recruiting
St. Bernards Heart and VascularJonesboro, Arkansas, United StatesRecruiting
UC San Diego HealthLa Jolla, California, United StatesNot Yet Recruiting
Providence Medical FoundationOrange, California, United StatesNot Yet Recruiting
Cedars-Sinai Medical CenterSanta Monica, California, United StatesNot Yet Recruiting
MedStar Washington Hospital CenterWashington D.C., District of Columbia, United StatesNot Yet Recruiting
Mount Sinai Medical Center of FloridaMiami Beach, Florida, United StatesNot Yet Recruiting
AdventHealthOrlando, Florida, United StatesNot Yet Recruiting
Emory UniversityAtlanta, Georgia, United StatesNot Yet Recruiting
Endeavor HealthGlenview, Illinois, United StatesNot Yet Recruiting
Baptist HealthLexington, Kentucky, United StatesNot Yet Recruiting
John Hopkins MedicalBaltimore, Maryland, United StatesNot Yet Recruiting

+ 23 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07324031