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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01669551
Other study ID # UPenn 815656
Secondary ID
Status Completed
Phase N/A
First received August 16, 2012
Last updated December 8, 2014
Start date July 2012
Est. completion date December 2014

Study information

Verified date August 2012
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study will compare 3 dimensional intracardiac echo (ICE) with 2 dimensional ICE or transesophageal echo in patients with structural and valvular heart disease who are already scheduled to undergo a percutaneous intervention. Specifically those patients would be those scheduled for a PFO or ASD repair, mitral balloon valvuloplasty, diagnostic cardiac catheterization assessment of aortic stenosis and those undergoing transcatheter aortic valve replacement.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 2014
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients in the study population referred to the cardiac catheterization laboratory for a percutaneous procedure to treat structural or valvular heart disease

Exclusion Criteria:

- Class IV CHF, inadequate femoral access, coagulation abnormalities, intracariac thrombus or DVT

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Pennsylvania

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison of volume intracardiac echo imaging to 2 dimensional echo Comparison study No