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Cardiac Computed Tomography (CT) Scan Compared to Transesophageal Echocardiogram (TEE) in Endocarditis

This study has been terminated.
(Difficult recruitment)
Sponsor:
ClinicalTrials.gov Identifier:
NCT00995384
First Posted: October 15, 2009
Last Update Posted: March 22, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Lihua QU, William Beaumont Hospitals
  Purpose
The purpose of this study is to assess the effectiveness of cardiac CT versus TEE in endocarditis patients.

Condition Intervention
Endocarditis Procedure: CT Scan

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Diagnostic
Official Title: A Novel Modality of Cardiac CT in Characterization of Acute Infective Endocarditis

Resource links provided by NLM:


Further study details as provided by Lihua QU, William Beaumont Hospitals:

Primary Outcome Measures:
  • Visual Difference in CT versus TEE images in Endocarditis [ Time Frame: Upon CT Scan ]

Secondary Outcome Measures:
  • Morbidity [ Time Frame: 4 weeks & 6 months post CT scan ]

Enrollment: 2
Study Start Date: October 2009
Study Completion Date: October 2010
Primary Completion Date: October 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
CT scan
CT Scan for endocarditis patients. All patients receive intervention.
Procedure: CT Scan
Cardiac CT with special attention to valves in Endocarditis patients.

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Acute endocarditis with positive TEE

Exclusion Criteria:

  • Renal failure
  • Contrast dye allergy
  • Beta-blocker allergy
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00995384


Locations
United States, Michigan
William Beaumont Hosptial
Royal Oak, Michigan, United States, 48073
Sponsors and Collaborators
William Beaumont Hospitals
Investigators
Principal Investigator: Phillip Kadaj, MD William Beaumont Hospitals
  More Information

Responsible Party: Lihua QU, Coordinator, William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00995384     History of Changes
Other Study ID Numbers: HIC 2009-148
R/C# 98699
RI-09-17
First Submitted: October 14, 2009
First Posted: October 15, 2009
Last Update Posted: March 22, 2012
Last Verified: March 2012

Additional relevant MeSH terms:
Endocarditis
Heart Diseases
Cardiovascular Diseases