X-ray Dose Reduction Study for Cardiac Angiography and Intervention
Primary Purpose
Vascular Diseases
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Angiographic run with new algorithm and low dose (50% dose)
Angiographic run with predecessor algorithm and dose (100%)
Sponsored by
About this trial
This is an interventional treatment trial for Vascular Diseases focused on measuring X-rays, Image processing, Cardiovascular procedure
Eligibility Criteria
Inclusion Criteria:
- Patients older than 18 years of age undergoing coronary angiography
Exclusion Criteria:
- Patients not willing or unable to give consent to participate
- Patients already involved in a clinical trial
- Patients under the age of 18
- Pregnant women and breastfeeding women
- Patients with severe kidney disease (eGFR < 60)
Sites / Locations
- Radboud University Nijmegen Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
ClarityIQ
AlluraXper
Arm Description
Angiographic run with new algorithm and low dose (50% dose)
Angiographic run with predecessor algorithm and dose (100% dose)
Outcomes
Primary Outcome Measures
Image Quality
Overall proportion where diagnostic image quality of ClarityIQ is scored equal or better compared to AlluraXper by the blinded readers. Reading is performed by simultaneous visual comparison of the image quality of AlluraXper and ClarityIQ by multiple blinded reviewers.The images are presented in a randomized order.
The hypothesis is that the overall proportion where diagnostic image quality of ClarityIQ is scored equal or better is ≥ than 0.80. Combined for all raters, the lower bound of the one-sided 95% CI (lower bound of the two-sided 90% CI)is used.
Secondary Outcome Measures
Radiation Dose Measurements: Dose Area Product (DAP)
Percentage of change of ClarityIQ vs. AlluraXper in Dose Area Product (DAP) calculated by DAP/frame. Negative percentage means a reduction in dose for ClarityIQ vs. AlluraXper.
Full Information
NCT ID
NCT01684826
First Posted
September 11, 2012
Last Updated
March 7, 2022
Sponsor
Philips Clinical & Medical Affairs Global
1. Study Identification
Unique Protocol Identification Number
NCT01684826
Brief Title
X-ray Dose Reduction Study for Cardiac Angiography and Intervention
Official Title
Clinical Validation and Evaluation of ClarityIQ Cardiac Image Processing for Cardiac Angiography and Intervention
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Philips Clinical & Medical Affairs Global
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Diseases
Keywords
X-rays, Image processing, Cardiovascular procedure
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ClarityIQ
Arm Type
Experimental
Arm Description
Angiographic run with new algorithm and low dose (50% dose)
Arm Title
AlluraXper
Arm Type
Experimental
Arm Description
Angiographic run with predecessor algorithm and dose (100% dose)
Intervention Type
Radiation
Intervention Name(s)
Angiographic run with new algorithm and low dose (50% dose)
Other Intervention Name(s)
ClarityIQ
Intervention Description
Angiographic run with new algorithm and low dose (50% lower dose compared to Xper)
Intervention Type
Radiation
Intervention Name(s)
Angiographic run with predecessor algorithm and dose (100%)
Other Intervention Name(s)
AlluraXper
Intervention Description
Angiographic run with predecessor algorithm and dose (100% dose)
Primary Outcome Measure Information:
Title
Image Quality
Description
Overall proportion where diagnostic image quality of ClarityIQ is scored equal or better compared to AlluraXper by the blinded readers. Reading is performed by simultaneous visual comparison of the image quality of AlluraXper and ClarityIQ by multiple blinded reviewers.The images are presented in a randomized order.
The hypothesis is that the overall proportion where diagnostic image quality of ClarityIQ is scored equal or better is ≥ than 0.80. Combined for all raters, the lower bound of the one-sided 95% CI (lower bound of the two-sided 90% CI)is used.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Radiation Dose Measurements: Dose Area Product (DAP)
Description
Percentage of change of ClarityIQ vs. AlluraXper in Dose Area Product (DAP) calculated by DAP/frame. Negative percentage means a reduction in dose for ClarityIQ vs. AlluraXper.
Time Frame
Participants were followed for the duration of the procedure
Other Pre-specified Outcome Measures:
Title
Radiation Dose Measurements: Air Kerma (AK)
Description
Percentage of change of ClarityIQ vs. AlluraXper in Air Kerma (AK) calculated by AK/frame. Negative percentage means a reduction in dose for ClarityIQ vs. AlluraXper.
Time Frame
Participants were followed for the duration of the procedure
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients older than 18 years of age undergoing coronary angiography
Exclusion Criteria:
Patients not willing or unable to give consent to participate
Patients already involved in a clinical trial
Patients under the age of 18
Pregnant women and breastfeeding women
Patients with severe kidney disease (eGFR < 60)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harry Suryapranata, Prof Dr.
Organizational Affiliation
Radboud University Nijmegen Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Center
City
Nijmegen
ZIP/Postal Code
6500HB
Country
Netherlands
12. IPD Sharing Statement
Learn more about this trial
X-ray Dose Reduction Study for Cardiac Angiography and Intervention
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