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Long-Term Follow-Up of Patients Undergoing Catheter Ablation

NCT ID: NCT00584558

Last Updated: 2017-10-02

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

2420 participants

Study Classification

OBSERVATIONAL

Study Start Date

2001-02-28

Study Completion Date

2016-06-08

Brief Summary

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The purpose of this study is to assess the long-term effects of catheter ablation procedures performed at the OU Medical Center.

Detailed Description

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The purpose of this study is to assess the long-term effects of catheter ablation procedures performed at this institution, including recurrence of the ablated arrhythmia and any late complications.

Conditions

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Arrhythmia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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1

Patients undergoing catheter ablation.

Catheter Ablation

Intervention Type PROCEDURE

Catheter Ablation of arrhythmias

Interventions

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Catheter Ablation

Catheter Ablation of arrhythmias

Intervention Type PROCEDURE

Other Intervention Names

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All approved ablation catheters Investigational ablation catheters

Eligibility Criteria

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Inclusion Criteria

* Undergoing catheter ablation at the OU Medical Center

Exclusion Criteria

* Prisoners
* Refusal to participate
Minimum Eligible Age

1 Year

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Oklahoma

OTHER

Sponsor Role lead

Responsible Party

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Karen Beckman, MD

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Karen Beckman, MD

Role: PRINCIPAL_INVESTIGATOR

University of Oklahoma

Locations

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OU Medical Center

Oklahoma City, Oklahoma, United States

Site Status

Countries

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United States

Other Identifiers

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1239

Identifier Type: -

Identifier Source: org_study_id