The primary objective of this study is to determine if a novel lead-based arm board is effective at reducing radiation dose to the operator during invasive cardiac procedures. Secondary objectives are to measure effect on radiation dose to patient and total fluoroscopy (x-ray) time.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
360
Novel Lead Based Armboard
Standard Armboard (without lead)
London Health Sciences Centre
London, Ontario, Canada
Radiation dose (μSv) to the operator at the chest
Co-primary outcomes included radiation dose (μSv; mean ± SD) to the operator at the chest and forearm level.
Time frame: At procedure completion
Radiation dose (μSv) to the operator at the forearm level
Co-primary outcomes included radiation dose (μSv; mean ± SD) to the operator at the chest and forearm level.
Time frame: At procedure completion
Air kerma
Time frame: At procedure completion
Dose area product
Time frame: At procedure completion
Radiation dose to the patient
Time frame: At procedure completion
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