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

This study has been terminated.

(PI stopped study to make a more substantial database.)

Sponsor:

Information provided by (Responsible Party):

Emile Daoud, The Ohio State University

ClinicalTrials.gov Identifier:

NCT00825968

First received: January 16, 2009

Last updated: September 16, 2011

Last verified: September 2011

History of Changes

Purpose

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

Condition
Heart Disease Atrial Fibrillation

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Prospective
Official Title:	Data Collection and Analysis of Patients Who Have Had an Electrophysiological Procedure Performed at the Ross Heart Hospital

Resource links provided by NLM:

Genetics Home Reference related topics: familial atrial fibrillation

MedlinePlus related topics: Atrial Fibrillation Heart Diseases

U.S. FDA Resources

Further study details as provided by Ohio State University:

Enrollment:	58
Study Start Date:	July 2008
Study Completion Date:	July 2009
Primary Completion Date:	December 2008 (Final data collection date for primary outcome measure)

Groups/Cohorts
Data collection group Patients having procedures done at the electrophysiology Laboratories at the Ross Heart Hospital at The Ohio State University Medical Center.

Detailed 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.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Female
Accepts Healthy Volunteers:	No
Sampling Method:	Non-Probability Sample

Study Population

Patients having procedures completed at the electrophysiology Laboratories at the Ross Heart Hospital at The Ohio State University Medical Center.

Criteria

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:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00825968

Locations

United States, Ohio
The Ohio State University Medical Center
Columbus, Ohio, United States, 43210

Sponsors and Collaborators

Emile Daoud

Investigators

Principal Investigator:

Emile Daoud, MD

Ohio State University

More Information

No publications provided

Responsible Party:	Emile Daoud, Professor, The Ohio State University
ClinicalTrials.gov Identifier:	NCT00825968 History of Changes
Other Study ID Numbers:	2008H0013
Study First Received:	January 16, 2009
Last Updated:	September 16, 2011
Health Authority:	United States: Institutional Review Board

Keywords provided by Ohio State University:

Electrophysiological
Heart Disease
Cardiology
Atrial Fibrillation

Risk Factors
Follow-up
Outcomes

Additional relevant MeSH terms:

Atrial Fibrillation
Heart Diseases
Arrhythmias, Cardiac
Cardiovascular Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on June 18, 2013

To Top