LifeVac Survey Study
Completed
Conditions studied: Airway Obstruction, Choking
In brief
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.
Key facts
- Study ID
- NCT06659796
- Run by
- LifeVac, LLC
- People needed
- 2930
- Starts
- 2024-06-24
- Expected to finish
- 2025-01-31
- Last updated by the study team
- 2025-07-18
Who can join
Age: 1 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Purchases of the LifeVac device Original database: all purchasers of the LifeVac device from the LifeVac website starting in 2015 until April 2024, a timeframe that yields a database of above 450,000 individuals with no email duplications and third party suppliers.
- Survey batches: randomly selected sample of 50,000 purchasers (10% of the database).
- Number of batches required will be based on response rate.
- English speaking
- Ability to understand and accept the consent form
You may not qualify if…
- Did not purchase a LifeVac device
- Third party suppliers
- Non-English speakers (as LifeVac labeling and survey materials are only available in English)
- Unwilling or unable to accept the consent form
Where it is running
- Boston MedTech Advisors — Dedham, Massachusetts, United States
Full record on ClinicalTrials.gov
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