Brief Title
X-ray Fluoroscopy Fused With Computed Tomography (XFC) Technical Development
Official Title
X-ray Fluoroscopy Fused With Computed Tomography (XFC) Technical Development
Brief Summary
Background: - Computed tomography (CT) creates three-dimensional images based on X-ray imaging. CT is useful for determining treatment approaches for certain diseases, such as calcific aortic stenosis (narrowing of the aorta because of calcium deposits). - Comparing the data received from CT scans with the data received from heart catheterization (which assesses the heart's condition and function) can be used to improve treatment in patients with certain heart conditions. Researchers are interested in looking at the effectiveness of both procedures in assessing possible surgical treatments for patients with calcific aortic stenosis. Objectives: - To analyze cardiac CT scans in conjunction with existing heart scan results to improve treatments for future minimally invasive aortic valve replacement. Eligibility: - Patients 18 years of age and older who have been diagnosed with aortic valve stenosis that may be treated surgically, and who will undergo or have recently undergone heart catheterization. Design: - Participants will have a CT scan within 90 days of the medically necessary heart catheterization, but before any other surgical or catheter treatment. - During the CT scan, patients will be asked to hold their breath intermittently for about 5 to 20 seconds. Patients will be inside the scanner for less than 30 minutes. - Patients will be asked to return in 3 to 7 days for a blood test to check kidney function. - Researchers will analyze the results of the CT scan in conjunction with the previous results from the catheterization to determine possible improved treatment options.
Detailed Description
We will collect cardiac computed tomography (CT) data from patients with aortic valve stenosis being considered for surgical or catheter treatment. These data will be analyzed along with medically-necessary fluoroscopy from cardiac catheterization to learn whether they can be combined to enhance future minimally invasive valve treatments.
Study Type
Observational
Condition
Aortic Valve Stenosis
Publications
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
Recruitment Information
Estimated Enrollment
1
Start Date
August 6, 2009
Completion Date
May 27, 2010
Eligibility Criteria
- INCLUSION CRITERIA: SELECTION CRITERIA: PATHWAY FOR RESEARCH CT: - Adult patients age 18 years or older - Having calcific aortic stenosis being considered for surgical or catheter-based treatment, determined on physical examination or noninvasive imaging such as echocardiography - Undergoing diagnostic cardiac catheterization within 1 year - Able to provide informed consent ALTERNATIVE SELECTION CRITERIA: PATHWAY FOR ANALYSIS OF MEDICAL DATA: - Adult patients age 18 years or older - Having calcific aortic stenosis being considered for surgical or catheter-based treatment, determined on physical examination or noninvasive imaging such as echocardiography - Undergoing diagnostic cardiac catheterization within 1 year - Having undergone cardiac CT for medical indications meeting the technical requirements of this protocol - Able to provide informed consent EXCLUSION CRITERIA: SELECTION CRITERIA: PATHWAY FOR RESEARCH CT: - Pregnant or lactating women - Decompensated heart failure (unable to lie flat during CT) EXCLUSION CRITERIA FOR BETA ADRENERGIC BLOCKERS: - Advanced atrioventricular block (Mobitz Type II second degree or third degree atrioventricular heart block) - Asthma or chronic obstructive pulmonary disease (emphysema) currently treated with beta adrenergic agonists EXCLUSION CRITERIA FOR IODINATED RADIOCONTRAST: -Severe kidney disease (MDRD estimated Glomerular Filtration Rate < 30mL/min/l.73m(2)). -Request of referring physician or surgeon not to administer iodinated radiocontrast ALTERNATIVE SELECTION CRITERIA: PATHWAY FOR ANALYSIS OF MEDICAL DATA: -None
Gender
All
Ages
18 Years - N/A
Accepts Healthy Volunteers
No
Contacts
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Location Countries
United States
Location Countries
United States
Administrative Informations
NCT ID
NCT00965679
Organization ID
090211
Secondary IDs
09-H-0211
Study Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Study Sponsor
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Verification Date
May 27, 2010