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NCT00825968 Clinical Trial

Data Collection and Analysis of Patients Who Have Had an Electrophysiological Procedure

Atrial Fibrillation Clinical Trial

Official title:
Data Collection and Analysis of Patients Who Have Had an Electrophysiological Procedure Performed at the Ross Heart Hospital

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00825968
Other study ID # 2008H0013
Secondary ID
Status Terminated
Phase N/A
First received January 16, 2009
Last updated September 16, 2011
Start date July 2008
Est. completion date July 2009

Study information
Verified date September 2011
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of the database is to complete outcomes research of electrophysiological procedures.

Description:

The purpose of the database is to complete outcomes research (risk factors, follow-up, procedural data) Perhaps the most important research for any busy clinical laboratory is to appreciate the tendencies and trends that are occurring in their own laboratory setting. This will have a tremendous impact on educating the OSU staff as well as perhaps other centers on best medical practices.

Recruitment information / eligibility
Status Terminated
Enrollment 58
Est. completion date July 2009
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age and older

- have or had a procedure preformed in the Electrophysiology Laboratories at the Ross Heart Hospital

- Ability to consent

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States The Ohio State University Medical Center Columbus Ohio

Sponsors (1)
Lead Sponsor Collaborator
Emile Daoud

Country where clinical trial is conducted

United States, 

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