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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02733913
Other study ID # PVI
Secondary ID
Status Completed
Phase N/A
First received February 18, 2016
Last updated November 9, 2017
Start date August 2014
Est. completion date March 31, 2017

Study information

Verified date November 2017
Source Heinrich-Heine University, Duesseldorf
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pulmonary vein isolation (PVI) has become a standard therapy for atrial fibrillation (AF), however, there is still considerable AF recurrence after PVI. Except for PV-left atrium (LA) reconnection, the cause of recurrence has been not yet fully clarified.

The alternation of autonomic tone plays an important role in initiation of paroxysmal AF. It was reported that there are multiple gangliated plexus (GP) around pulmonary veins, therefore the modulation targeting those GPs, resulting in modulations of cardiac autonomic tone, have been conducted. Some study showed the efficacy of GP ablation for AF patients.

According to the previous reports, heart rate (HR) increased, and heart rate variability (HRV) reduced after PVI. These are considered to be due to "autonomic denervation" caused by catheter ablation of GP.

For the best of investigators knowledge, there have been no data on heart rate turbulence (HRT) of baroreflex sensitivity (BRS) concerning PVI.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date March 31, 2017
Est. primary completion date March 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients who undergo PVI for paroxysmal atrial fibrillation

- Patients in sinus rhythm at baseline

Exclusion Criteria:

- prior left atrial Ablation

- left atrial diameter >55mm

- frequent atrial extrasystole, frequent ventricular Extrasystole

- Diabetes Mellitus

- sleep apnea syndrome

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Division of Cardiology, Pulmonary Disease and Vascular Medicine Düsseldorf

Sponsors (1)

Lead Sponsor Collaborator
Klinik für Kardiologie, Pneumologie und Angiologie

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary recurrence of AF Time measured in days to recurrence of AF 12 months
Secondary effect of PVI on cardiac autonomic system utilizing HRT measurement 12 months
Secondary effect of PVI on cardiac autonomic system utilizing BRS measurement 12 months
Secondary association between measured parameters (HRT, BRS) and the recurrence of AF 12 months
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