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Impact of Low Frame Rate Fluoroscopy and Cine-angiography on Reducing Operator and Patient Dose

Primary Purpose

Stable Angina, Unstable Angina, Acute Coronary Syndrome

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Radiation: 15 FPS Cine 15 PPS
Radiation: 7.5 low Frame rate
Low Cine
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Stable Angina focused on measuring radiation, fluoroscopy, diagnostic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing elective or urgent cardiac catheterisation with or without ad-hoc PCI or planned PCI in the pre-specified catheterisation laboratories.

Exclusion Criteria:

  • Patients who undergo procedures other than diagnostic coronary angiography or intervention (e.g. electrophysiological procedures).
  • Patients participating in other research study requiring higher cine angiography.
  • ST-elevation Myocardial Infarction

Sites / Locations

  • University Health Network - Peter Munk Cardiac Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

Conventional rate fluoroscopy

Intermediate frame rate 7.5 fps

Low frame rate

Arm Description

Radiation: 15 FPS Cine 15 PPS

Radiation: 7.5 low Frame rate

Low Cine 10 PPS

Outcomes

Primary Outcome Measures

Radiation Exposure to patient
Radiation exposure to patient will be measured by Dose-Area product (DAP) collected during the procedure.

Secondary Outcome Measures

Image quality assessment of the coronary angiogram
Coronary angiograms will be assessed by blinded operators for quality of image using a pre-specified tool

Full Information

First Posted
May 26, 2015
Last Updated
October 13, 2015
Sponsor
University Health Network, Toronto
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1. Study Identification

Unique Protocol Identification Number
NCT02574949
Brief Title
Impact of Low Frame Rate Fluoroscopy and Cine-angiography on Reducing Operator and Patient Dose
Official Title
Impact of Low Frame Rate Fluoroscopy and Cine-angiography on Reducing Operator and Patient Radiation Dose and Impact on Image Quality During Cardiac Catheterization
Study Type
Interventional

2. Study Status

Record Verification Date
October 2015
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (undefined)
Primary Completion Date
July 2016 (Anticipated)
Study Completion Date
July 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Health Network, Toronto

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators sought to investigate the efficacy of low frame rate (fluoroscopy at 7.5 frames per second (FPS) and Cine at 10 pulse per second (PPS) vs. conventional (15 FPS and 15 PPS) on radiation dose to the patient and the operator during coronary angiography and intervention. In addition, investigators sought to qualitatively assess the effect, if any, of the low frame rate on angiographic image quality.
Detailed Description
Minimizing radiation exposure to patient and the operator is considered one of the primary safety concerns in the catheterization laboratory. Patients undergoing diagnostic angiography +/- ad hoc PCI or planned PCI, will be randomised to conventional settings (15 FPS and 15 PPS) or low frame rate settings (7.5 FPS and 15 PPS) or low Cine settings (7.5 FPS and 10 PPS). The patient radiation dose, patient radiation dose area product (DAP), and fluoroscopy time will be measured. Statistical Analysis: Demographic and procedural variables will be presented as percentage (categorical variable) or mean ± SD (continuous variable). Patients will be randomized into three arms - a control arm and two intervention arms. The angiographic radiation protocol will adhere to standard practice in both fluoroscopy and cine images at 15 frames/second. The intervention arm will consist of two groups. Group 1 with fluoroscopy images set at 7.5 frames/second and cine images set at 15 frames/second and group 2 with fluoroscopy set at 7.5 frames/second and cine set at 10 frames/second. Sample size calculations are based on assuming a reduction in radiation dose in group 1 of 10% and in group 2 of 20%. At 5% significance and 80% power, a sample size of 200 patients will be required in each intervention arm. Allowing for a 10% attrition rate, a sample size of 220 patients will be required in each intervention arm with 100 patients in the control arm.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stable Angina, Unstable Angina, Acute Coronary Syndrome
Keywords
radiation, fluoroscopy, diagnostic

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional rate fluoroscopy
Arm Type
Active Comparator
Arm Description
Radiation: 15 FPS Cine 15 PPS
Arm Title
Intermediate frame rate 7.5 fps
Arm Type
Experimental
Arm Description
Radiation: 7.5 low Frame rate
Arm Title
Low frame rate
Arm Type
Experimental
Arm Description
Low Cine 10 PPS
Intervention Type
Radiation
Intervention Name(s)
Radiation: 15 FPS Cine 15 PPS
Other Intervention Name(s)
Conventional
Intervention Description
Radiation 15 FPS Cine 15 PPS
Intervention Type
Radiation
Intervention Name(s)
Radiation: 7.5 low Frame rate
Other Intervention Name(s)
Low rate fluoroscopy
Intervention Description
Radiation: Frame rate 7.5 FPS, Cine 15 PPS
Intervention Type
Radiation
Intervention Name(s)
Low Cine
Other Intervention Name(s)
Low pulse rate Cine
Intervention Description
Radiation: Frame rate 7.5 FPS, Cine 10 PPS
Primary Outcome Measure Information:
Title
Radiation Exposure to patient
Description
Radiation exposure to patient will be measured by Dose-Area product (DAP) collected during the procedure.
Time Frame
During Cardiac catheterization procedure
Secondary Outcome Measure Information:
Title
Image quality assessment of the coronary angiogram
Description
Coronary angiograms will be assessed by blinded operators for quality of image using a pre-specified tool
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing elective or urgent cardiac catheterisation with or without ad-hoc PCI or planned PCI in the pre-specified catheterisation laboratories. Exclusion Criteria: Patients who undergo procedures other than diagnostic coronary angiography or intervention (e.g. electrophysiological procedures). Patients participating in other research study requiring higher cine angiography. ST-elevation Myocardial Infarction
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Divyesh Sharma, MSc,MRCP
Phone
001-647-961-9336
Email
divyeshsharma11@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ashish H Shah, MD, MD(Res)
Phone
001-416-835-2822
Email
ashish.shah@uhn.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir Dzavik, MD, FRCPC
Organizational Affiliation
UHN, Toronto, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network - Peter Munk Cardiac Centre
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

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Impact of Low Frame Rate Fluoroscopy and Cine-angiography on Reducing Operator and Patient Dose

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