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LifeVac Survey Study

NCT06659796 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2930

Last updated 2025-07-18

No results posted yet for this study

Summary

This observational, non-interventional survey study is intended to explore user experiences with the LifeVac airway clearance device, with a particular emphasis on real-world application in choking emergencies in the USA. This study seeks to gather valuable insights from a representative sample of the LifeVac device purchaser base.

The main questions the study aims to answer are:

1. Is the LifeVac device safe for individuals experiencing a choking emergency?
2. Is the LifeVac device successful in removing an obstruction during a choking incident?

Participants: Purchasers of the LifeVac device.

Conditions

  • Airway Obstruction
  • Choking

Interventions

DEVICE

LifeVac

Removal of airway obstruction during choking emergency

Sponsors & Collaborators

  • LifeVac, LLC

    lead INDUSTRY

Principal Investigators

  • Andrea Nadai · Boston MedTech Advisors

Eligibility

Min Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-24
Primary Completion
2025-01-31
Completion
2025-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06659796 on ClinicalTrials.gov