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Reducing the effective radiation dose and the amount of contrast medium in CTA of the abdominal aorta

Reducing the effective radiation dose and the amount of contrast medium in CTA of the abdominal aorta - Radiation dose and contrast reduction in CTA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON36968
Enrollment
30
Registered
2012-10-30
Start date
2012-11-01
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Bloodvessel deviations

Interventions

Randomly, 15 Patients are assigned to undergo the CARE kV protocol using the Combined Applications to Reduce Exposure (CARE kV) tool of Siemens, CARE kV automatically suggest kV and effective mAs to
a tube current of 120 kV and 100 ml contrast medium [9]. In our previous study we used a test bolus reduction protocol with a test bolus of 10 mL contrast medium (ioversol 350, 350 mg iodine per mi
Optiray 350, Tyco Health care, Mansfield, Mass) to synchronize the data acquisition with the arrival of contrast material in the abdominal aorta. The test bolus was followed by a bolus injection of

Sponsors

Jeroen Bosch Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Referred for CTA of the abdominal aorta according to clinical indications - Mentally competent - Signed informed consent - >= 18 years - Kidney function >= 60 GFR

Exclusion criteria

Exclusion criteria: -

Design outcomes

Primary

MeasureTime frame
The amount of Hounsfield Units (HU) measured in the aorta at 30 positions from the celiac trunk to the iliac arteries in both groups.

Secondary

MeasureTime frame
• The uniformity of the attenuation values of both protocols. • The clinical usefulness of the scans determined by 3 radiologists and scored at a scale from 1 to 5. • The effective radiation dose of the scans for both protocols • The contrast-to-noise-ratio of the scans for both protocols • The Signal tot noise ratio of the scans for both protocols

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)