RapidShock Post-Approval Study

ZOLL Medical

Status: Completed

Conditions: Cardiac Arrest

Treatments: Device: RapidShock

Study type: Interventional

Funder types: Industry

Identifiers

NCT04014842

12701

Details and patient eligibility

About

Compare the performance of the Reconfirmation Analysis Mode algorithm to the performance goals recommended by the American Heart Association.

Enrollment: 2,756 patients

Sex: All

Ages: 8+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 8 years of age or older and weight ≥ 55 lbs (25 kgs)
• Out-of-hospital cardiac arrest (OOHCA)
• Non-traumatic cardiac arrest

Exclusion criteria

• Weight less than 55 lbs (25 kgs)
• Do not attempt resuscitation (DNAR) orders

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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2,756 participants in 1 patient group

RapidShock

Other group

Description:

Patients receiving xseries device with rapid shock enabled

Treatment:

Device: RapidShock