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On Dose Efficiency of Modern CT-scanners in Chest Scans

On Dose Efficiency of Modern CT-scanners in Chest Scans- a Prospective, Randomized Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04996693
Enrollment
958
Registered
2021-08-09
Start date
2021-10-07
Completion date
2023-05-31
Last updated
2023-11-22

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

Conditions

Aortic Stenosis, Lung Cancer, Pneumonia, Pulmonary Disease, Pulmonary Embolism

Keywords

Spectral CT, Computed Tomography, Dose efficiency

Brief summary

CT scans of the chest / thorax are of great importance both in the initial diagnosis and in the follow-up of pulmonary or thoracic diseases. As an example, CT angiography of the pulmonary arteries (CTPA) is worldwide considered to be gold standard test in patients with a suspicion for pulmonary embolism. The aim of this study is to measure and compare dose efficiency of modern CT scanners for unenhanced and contrast-enhanced scan protocols of the chest/thorax. Patients who are referred for a CT of the chest/thorax will be randomly assigned to one of the three CT scanners currently in use at our institution.

Interventions

DIAGNOSTIC_TESTImaging on Scanner with Spectral Imaging Capabilities

Patients will undergo imaging on a modern CT scanner with spectral imaging capabilities. A dose neutral spectral acquisition mode will routinely be used. Contrast material protocol and scan ranges are similar in all three arms.

DIAGNOSTIC_TESTCT Scan using an Energy-Integrating Detector CT (128 slice MDCT)

Patients will undergo imaging on a modern 128-slice CT scanner (Siemens Healthineers) with energy-integrating detector and without spectral acquisition mode. Contrast material protocol and scan ranges are similar in all three arms.

DIAGNOSTIC_TESTCT Scan using an Energy-Integrating Detector CT (20-slice MDCT)

Patients will undergo imaging on a modern 20-slice CT scanner (Siemens Healthineers) with energy-integrating detector and without spectral acquisition mode. Contrast material protocol and scan ranges are similar in all three arms.

Sponsors

University Hospital Augsburg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

no masking required

Intervention model description

Randomization of patients referred for a CT scan of the thorax on one of three CT scanners routinely used for this purpose in our department

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient is referred for an unenhanced CT OR contrast-enhanced CT of the chest/thorax confirmed by a board-certified radiologist ('justifying indication' according to German/European radiation protection law) AND * patient is at least 18 years of age AND * patient (is able to give informed consent and) has given informed consent.

Exclusion criteria

* high degree of medical urgency (i.e. patient cannot be consented for iv contrast according to routine procedures) * known or suspected pregnancy, or lactating . contraindications for contrast agent (renal failure, allergy, hyperthyroidism)

Design outcomes

Primary

MeasureTime frameDescription
Parameters of Objective Image Quality1 yearMeasured as signal, image noise and modulation transfer function equivalent parameters
Parameters of Radiation Dose1 yearmeasured as x-ray tube parameters such as dose length product (DLP)

Secondary

MeasureTime frameDescription
Subjective Image Quality Evaluation (entire cohort and for individual disease groups)1 yearmeasured by blinded evaluation by radiologists

Countries

Germany

Outcome results

None listed

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