NCT00618683

Completed

AV Nodal Reentrant Tachycardia Study

University of Oklahoma Source

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Other study identifiers

Sponsor study identifier

2353

Secondary identifiers

AHA

OTHER · American Heart Association

Study Type

interventional

Actual enrollment (reported)

46

Locations

1 country

Sites

1

Timeline

Study Start

March 25, 2004

Actual (reported)

Primary Completion

January 21, 2020

Actual (reported)

Study Completion

January 12, 2021

Actual (reported)

Brief Summary

The purpose of this study is to determine/identify what mechanisms/factors are involved with regard to AV nodal reentrant tachycardia.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Actual enrollment (reported): 46 participants
Study completion date: January 12, 2021
Actual (reported)
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
March 25, 2004
Actual (reported)
First Submitted
February 7, 2008
Actual (reported)
First Posted
February 20, 2008
Actual (reported)
Primary Completion
January 21, 2020
Actual (reported)
Study Completion
January 12, 2021
Actual (reported)

Last Updated: May 10, 2024
Status Verified: May 2024
Last Update Submitted: May 9, 2024

Conditions

Tachycardia, Atrioventricular Nodal Reentry

Keywords

AVNRTAtrioventricularnodal reentrant circuitnodal reentrant tachycardiaParoxysmal supraventricular tachycardia

Outcome Measures

Primary Outcomes (1)

raise the frequency of success to more than 98%
unk

Study Arms (1)

Study Arm

OTHER

Mapping and Ablation

Procedure: Cardiac Invasive Electrophysiological Study

Interventions

Cardiac Invasive Electrophysiological StudyProcedure

Mapping and localizing of the components of the reentrant circuit as part of the Electrophysiological Study

Study Arm

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age16 Years - 80 Years

Sexall

Healthy VolunteersNo

Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

Ages 16-80
At least one documented episode of AV nodal reentrant tachycardia

Sponsors & Collaborators

University of Oklahoma
Otherlead

Study Sites (1)

The University of Oklahoma Health Sciences Center

Oklahoma City, Oklahoma, 73104, United States

MeSH Terms

Conditions

Tachycardia, Atrioventricular Nodal ReentryTachycardia, Ventricular

Condition Hierarchy (Ancestors)

Tachycardia, ReciprocatingTachycardiaArrhythmias, CardiacHeart DiseasesCardiovascular DiseasesCardiac Conduction System DiseasePathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

Stavros Stavrakis, MD
University of Oklahoma
PRINCIPAL INVESTIGATOR

Enrollment

46 participants (actual enrollment reported by the registry).

Study Design

Study Type: interventional
Phase: not applicable
Allocation: NA
Masking: NONE
Purpose: DIAGNOSTIC
Intervention Model: SINGLE GROUP
Sponsor Type: OTHER
Responsible Party: SPONSOR

Study Record Dates

First Submitted

February 7, 2008

First Posted

February 20, 2008

Study Start

March 25, 2004

Actual (reported)

NCT05531903

High-density Activation Mapping of the Slow Pathwayto Guide Catheter Ablation in Patients With Typical Atrioventricular Nodal Reentrant Tachycardia

Not ApplicableCompleted

NCT05705297

Intracardiac Echocardiography Guided Slow Pathway Cryoablation

Enrolling By Invitation

NCT05296954

Localization of Anatomical Structures Involved in Nodal Tachycardias by High Density Mapping.

Not ApplicableRecruiting

NCT06492499

Patient-Centric Innovation: Superior Vena Cava Approach in Zero-Fluoroscopy

Completed

NCT07630480

3D Mapping Versus Conventional Ablation in AVNRT

Not ApplicableCompleted

NCT04764123

Typical and Atypical AVNRT High-resolution Mapping

Unknown

Patient scheduled for electrophysiology study and catheter ablation for supraventricular tachycardia

You may not qualify if:

Ages \< 16 or \> 80
Medical condition significantly increasing risk of extending procedure time or X-ray exposure
Pregnancy
Prior ablation with radiation exposure \>2 hours
Electrophysiology study performed without sedation or anesthesia
Unavailable for follow-up

Contact the study team to confirm eligibility.

Primary Completion

January 21, 2020

Actual (reported)

Study Completion

January 12, 2021

Actual (reported)

Last Updated

May 10, 2024

Record last verified: 2024-05

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00618683
Data provider: ClinicalTrials.gov
Source updated: 2024-05-10
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:19:03 UTC

Locations

US(1)

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

First Submitted

First Posted

Primary Completion

Study Completion

Conditions

Keywords

Outcome Measures

Primary Outcomes (1)

Study Arms (1)

Study Arm

Interventions

Eligibility Criteria

You may qualify if:

Sponsors & Collaborators

Study Sites (1)

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Enrollment

Study Design

Study Record Dates

You may not qualify if:

Source record

Locations