Trials / Completed
CompletedNCT01780350
Assessment of the Implementation of the ResQGARD® Impedance Threshold Device by the San Antonio Fire Department
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 200 (actual)
- Sponsor
- Advanced Circulatory Systems · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is attached to a comprehensive quality assurance/quality improvement (QA/QI) program conducted by the Office of the medical director, and is designed to contribute to generalizable knowledge to determine effectiveness and tolerability of an FDA approved Impedance Threshold Device (ITD) device in a large urban emergency medical service (EMS) system. The cohort will comprise a convenience sample of patients that are being treated by EMS for a hypotensive emergency.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ResQGARD ITD | Patients eligible for the device will receive the ResQGARD attached to a facemask or mouthpiece. The patient will use the device, provided it is tolerated, until their blood pressure is stabilized as determined by EMS personnel. |
Timeline
- Start date
- 2012-04-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2013-01-31
- Last updated
- 2015-02-27
- Results posted
- 2015-02-27
Source: ClinicalTrials.gov record NCT01780350. Inclusion in this directory is not an endorsement.