Clinical Trials Directory

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

TypeNameDescription
RADIATIONAngiographic run with new algorithm and low dose (50% dose)Angiographic run with new algorithm and low dose (50% lower dose compared to Xper)
RADIATIONAngiographic 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.