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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03401931
Other study ID # HSJ_AIFIB_2017
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date January 9, 2018
Est. completion date January 9, 2018

Study information

Verified date April 2020
Source Hospital St. Joseph, Marseille, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

pilot clinical study, multicenter, prospective, open, nonrandomized


Description:

The hypothesis is that ablation targeting PVI alone for the treatment of persistent AF is less efficient that ablation targeting electrophysiologic areas with spatio-temporal-dispersion with or without PVI


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date January 9, 2018
Est. primary completion date January 9, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: major patient with an indication of AF or AT ablation -

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Hopital d'Aix en Provence Aix-en-Provence
France CHU Nice Nice
Netherlands Isala Hospital Zwolle Netherland

Sponsors (1)

Lead Sponsor Collaborator
Hospital St. Joseph, Marseille, France

Countries where clinical trial is conducted

France,  Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary AF termination conversion to sinus rhythm or stable atrial tachycardia during the ablation procedure
Secondary AT termination conversion to sinus rhythm during the ablation procedure
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