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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02099643
Other study ID # HSJ-2013-03
Secondary ID
Status Completed
Phase N/A
First received March 26, 2014
Last updated March 28, 2014
Start date December 2008
Est. completion date March 2014

Study information

Verified date March 2014
Source Hospital St. Joseph, Marseille, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Recent data has demonstrated that focal sources are determinant in human atrial fibrillation (AF) perpetuation.

The investigators sought to identify crucial areas for AF perpetuation during our routine electrogram (EGM)-based substrate ablation.


Recruitment information / eligibility

Status Completed
Enrollment 113
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Atrial Fibrilation

- Undergoing EGM-based substrate ablation

Exclusion Criteria:

- Age < 18

Study Design


Related Conditions & MeSH terms

  • Atrial Fibrilation Termination Endpoint

Locations

Country Name City State
France Hopital Saint Joseph Marseille
France Hôpital Privé Jacques Cartier; Massy
France Institut Mutualiste Montsouris; Paris
United Kingdom Morphology Unit Royal Brompton Hospital London;

Sponsors (1)

Lead Sponsor Collaborator
Hospital St. Joseph, Marseille, France

Countries where clinical trial is conducted

France,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Atria fibrillation termination during procedure conversion to atrial tachycardia (AT) or sinus rhythm 240 min
Secondary Crucial points Crucial points were defined by areas where ablation immediately extended the cycle length> 20% of AF CL, or regularized Atrial Fibrilation (AF) into Atrial Tachycardia (AT) or converted AF (or AT) into Sinus Rythm 240 min