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Clinical Trials/NCT03113539
NCT03113539CompletedNot Applicable

Low-dose, EKG-gated CT Validity for the Evaluation of Ascendant Aortic Aneurysm.

Université de Sherbrooke2 sites in 1 country66 target enrollmentStarted: April 12, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
66
Locations
2
Primary Endpoint
Measures validity (aorta diameter in mm from scan images)

Study Overview

Brief Summary

We will demonstrate the validity of measurements with a low-dose, EKG-gated CT without contrast in the ascending aorta evaluation, compared with the current Angio-CT measurements.

Detailed Description

The actual protocol used in aorta evaluation consist of two CT-scans on the same study. The first scan that detects calcifications is using parameters with low-dose current, non EKG-gated and without contrast. The second scan uses iodine-contrast, EKG-gating and higher current dose to obtain higher image quality of diagnostic value.

The study will optimize the first scan parameters and compare the measures of the aorta diameters from the standard protocol.

By modifying the first scan parameters, we would demonstrate that the follow-up of an aortic aneurysm can safely be made with lower radiation exposure.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
60 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • 60 years old and more
  • 85 bpm or less

Exclusion Criteria

  • aortic material
  • EKG gating not possible
  • aorta pathology (thrombus, dissection)

Arms & Interventions

Subjects awaiting for an aortic evaluation

Experimental

Subjects already waiting for an aortic evaluation, either a first diagnostic scan or follow-up of a known aneurysm.

Each subjects will have the two CT-scans on the same day.

Intervention: Modified Low-dose, EKG-gated CT without contrast for the evaluation of aortic aneurysm (Other)

Outcomes

Primary Outcomes

Measures validity (aorta diameter in mm from scan images)

Time Frame: 12 months

Comparing aorta diameters from the two modalities.

Secondary Outcomes

  • Radiation (in msev from scanner report)(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Paul Farand

MD, FRCPC, Professeur agréé, Directeur du service de cardiologie

Université de Sherbrooke

Study Sites (2)

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