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Reducing Radiation Exposure to Operators During Invasive Cardiac Procedures

NCT03605030 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 360

Last updated 2018-07-30

No results posted yet for this study

Summary

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.

Conditions

  • Patients Undergoing Invasive Cardiac Procedures
  • Radiation Exposure

Interventions

DEVICE

Novel Lead Based Armboard

Novel Lead Based Armboard

DEVICE

Standard Armboard

Standard Armboard (without lead)

Sponsors & Collaborators

  • Western University, Canada

    collaborator OTHER

  • London Health Sciences Centre

    lead OTHER

Principal Investigators

  • Pallav Garg, MBBS, MSc · London Health Sciences Centre, Western University, London, ON

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-29
Primary Completion
2018-01-25
Completion
2018-05-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03605030 on ClinicalTrials.gov