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Low-dose Gated CT Validity for the Evaluation of Ascendant Aortic Aneurysm.

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03113539
Enrollment
66
Registered
2017-04-13
Start date
2017-04-12
Completion date
2019-05-30
Last updated
2019-07-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ascendant Aortic Aneurysm

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.

Interventions

OTHERModified Low-dose, EKG-gated CT without contrast for the evaluation of aortic aneurysm

On the same day, the subject will do : 1. Modified low-dose, EKG-gated CT without contrast 2. Usual high-dose, EKG-gated CT with contrast Comparing aortic diameters from the two protocols.

Sponsors

Université de Sherbrooke
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to 100 Years
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)

Design outcomes

Primary

MeasureTime frameDescription
Measures validity (aorta diameter in mm from scan images)12 monthsComparing aorta diameters from the two modalities.

Secondary

MeasureTime frameDescription
Radiation (in msev from scanner report)12 monthsComparing radiation exposure with the two modalities

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026