Trials / Completed
CompletedNCT01684826
X-ray Dose Reduction Study for Cardiac Angiography and Intervention
Clinical Validation and Evaluation of ClarityIQ Cardiac Image Processing for Cardiac Angiography and Intervention
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Philips Clinical & Medical Affairs Global · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
ClarityIQ is a novel X-ray imaging technology, that combines advanced real-time image noise reduction algorithms, with state-of-the-art hardware to reduce patient entrance dose significantly. This is realized by anatomy-specific optimization of the full acquisition chain (grid switch, beam filtering, pulse width, spot size, detector and image processing engine) for every clinical task individually. Furthermore, smaller focal spot sizes and shorter pulses are used, which are known to positively influence image quality . The final effect on the clinical image quality is investigated in this study.
Detailed description
Fluoroscopically guided procedures are associated with a risk of radiation injury to the skin, caused by high peak skin dose. The increasingly complex nature of many of the interventions performed requires the use of significant amounts of radiation for their completion. Of particular relevance to dose reduction concerns are obese patients, for whom additional radiation is often necessary to obtained sufficient diagnostic quality, as well as patients suffering from chronic total coronary occlusions (CTO), for whom long procedures with extended radiation time and contrast usage are common. In order to introduce a dose reduction technology the most important aspect is to validate the diagnostic image information. Philips has developed a new algorithm that is capable to process images with similar image quality but acquired at lower dose.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| RADIATION | Angiographic run with new algorithm and low dose (50% dose) | Angiographic run with new algorithm and low dose (50% lower dose compared to Xper) |
| RADIATION | Angiographic run with predecessor algorithm and dose (100%) | Angiographic run with predecessor algorithm and dose (100% dose) |
Timeline
- Start date
- 2012-09-01
- Primary completion
- 2012-11-01
- Completion
- 2012-11-01
- First posted
- 2012-09-13
- Last updated
- 2022-03-08
- Results posted
- 2013-11-01
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT01684826. Inclusion in this directory is not an endorsement.