Trials / Completed
CompletedNCT01510353
Effect of a Real Time Radiation Monitoring Device on Radiation Exposure During Cardiac Catheterization
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 505 (actual)
- Sponsor
- North Texas Veterans Healthcare System · Federal
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to examine the impact of using a real time radiation exposure monitoring device on the patient and operator radiation exposure during cardiac catheterization. The hypothesis of the study is that use of a real time radiation exposure monitoring device during cardiac catheterization will decrease both patient and operator radiation exposure compared to no use of the monitoring device.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Radiation monitoring device | Radiation monitoring device (Bleeper Sv, Vertec Scientific Ltd, Berkshire, UK) that provides real-time auditory feedback on radiation exposure during cardiac catheterization |
Timeline
- Start date
- 2012-01-01
- Primary completion
- 2014-05-01
- Completion
- 2014-05-01
- First posted
- 2012-01-16
- Last updated
- 2014-07-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01510353. Inclusion in this directory is not an endorsement.