Trials / Completed
CompletedNCT01272453
Computed Tomography Dose Reduction Using Sequential or Fast Pitch Sprial Technique
Computed Tomography Dose Reduction Using Sequential or Fast Pitch Sprial Technique Employed in Cardiothoracic Imaging
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,640 (actual)
- Sponsor
- Gilbert L. Raff, MD · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, controlled observational trial of patients undergoing clinically indicated cardiothoracic computed tomography (CT), including pulmonary or aortic angiography and coronary CT angiography (CCTA).
Detailed description
The development of a novel CT scanner capable of sequential or fast-pitch spiral techniques in most patients (Siemens Definition Flash) represents a potentially crucial technical innovation at a particularly critical juncture. National healthcare systems are under pressure to deliver accurate and cost-effective diagnosis of an increasing number of patients and CT angiography in various settings is a proven, highly accurate technique that has been shown to improve diagnostic efficiency and reduce the cost of care. However, there has been increasing concern about the lifetime attributable risk of cancer from radiation related to diagnostic procedures. Such concern extends to other radiation-based procedures that contribute to the cumulative lifetime radiation exposure of patients. The Flash scanner holds the promise of substantially reducing exposure resulting from a variety of examinations. The CT DOSE multicenter trial is therefore designed to validate the extent of dose reduction attendant to the use of the Flash scanner in cardiothoracic scanning, and to determine whether image quality is preserved in spite of significant dose reduction.
Conditions
Timeline
- Start date
- 2011-01-01
- Primary completion
- 2013-10-01
- Completion
- 2013-10-01
- First posted
- 2011-01-07
- Last updated
- 2014-05-30
Locations
9 sites across 2 countries: United States, Saudi Arabia
Source: ClinicalTrials.gov record NCT01272453. Inclusion in this directory is not an endorsement.