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Data Collection and Analysis of Patients Who Have Had an Electrophysiological Procedure
This study is currently recruiting participants.
Verified by Ohio State University, January 2009
First Received: January 16, 2009   Last Updated: January 20, 2009   History of Changes
Sponsored by: Ohio State University
Information provided by: Ohio State University
ClinicalTrials.gov Identifier: NCT00825968
  Purpose

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


Condition
Heart Disease
Atrial Fibrillation

Genetics Home Reference related topics: Brugada syndrome familial atrial fibrillation short QT syndrome
MedlinePlus related topics: Atrial Fibrillation Heart Disease in Women Heart Diseases
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective
Official Title: Data Collection and Analysis of Patients Who Have Had an Electrophysiological Procedure Performed at the Ross Heart Hospital

Further study details as provided by Ohio State University:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 2500
Study Start Date: July 2008
Estimated Study Completion Date: December 2020
Estimated Primary Completion Date: December 2015 (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 Recruiting
Columbus, Ohio, United States, 43210
Contact: Kathryn Crow, RN     614-247-7847     Kathryn.Crow@osumc.edu    
Contact: Leah White, MPH     614-247-7133     Leah.White@osumc.edu    
Principal Investigator: Emile Daoud, MD            
Sponsors and Collaborators
Ohio State University
Investigators
Principal Investigator: Emile Daoud, MD Ohio State University
  More Information

No publications provided

Responsible Party: The Ohio State University ( Emile Daoud MD )
Study ID Numbers: 2008H0013
Study First Received: January 16, 2009
Last Updated: January 20, 2009
ClinicalTrials.gov Identifier: NCT00825968     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Ohio State University:
Electrophysiological
Heart Disease
Cardiology
Atrial Fibrillation
Risk Factors
Follow-up
Outcomes

Study placed in the following topic categories:
Heart Diseases
Atrial Fibrillation
Arrhythmias, Cardiac

Additional relevant MeSH terms:
Pathologic Processes
Heart Diseases
Cardiovascular Diseases
Atrial Fibrillation
Arrhythmias, Cardiac

ClinicalTrials.gov processed this record on May 07, 2009