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WithdrawnNCT03401931AI FibUpdated Apr 28, 2020

Artificial Intelligence Use for the Detection of Atrial Fibrillation Drivers

An observational study in Fibrillation, Atrial and To Evaluate the Intraoperative Efficiency of the AIFIB Software in the Detection of Atrial Fibrillation Driver During an Ablation Procedure, sponsored by Hospital St. Joseph, Marseille, France. Withdrawn at 3 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-04-28.

Sponsored by Hospital St. Joseph, Marseille, France · Observational

Why this study was withdrawn
another design of protocole is submitted for approuval before the start date
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
0
Ages
18 Years and older
Sex
All
01

Study summary

pilot clinical study, multicenter, prospective, open, nonrandomized

Read the detailed 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

02

Conditions studied

  • Fibrillation, Atrial
  • To Evaluate the Intraoperative Efficiency of the AIFIB Software in the Detection of Atrial Fibrillation Driver During an Ablation Procedure

Browse trials for

03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

major patient with an indication of AF or AT ablation

Eligibility criteria

Inclusion Criteria: major patient with an indication of AF or AT ablation -

Exclusion Criteria:

-

04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
0 participants (actual)
Target follow-up
2 Years
Patient registry
Yes
05

What researchers measure

Primary outcomes

  1. AF termination

    conversion to sinus rhythm or stable atrial tachycardia

    Time frame: during the ablation procedure

Secondary outcomes

  1. AT termination

    conversion to sinus rhythm

    Time frame: during the ablation procedure

06

Study locations

3 sites
  • Hopital d'Aix en Provence
    Aix-en-Provence, 13100, France
  • CHU Nice
    Nice, 06000, France
  • Isala Hospital
    Zwolle, Netherland, Netherlands
07

Registry details

Key details

Study ID
NCT03401931
Lead sponsor
Hospital St. Joseph, Marseille, France
Responsible party
SEITZ JULIEN (Cardiologist, Electrophysiology specialist, Hospital St. Joseph, Marseille, France) — Principal investigator
First posted
Jan 17, 2018
Start date
Jan 9, 2018
Primary completion
Jan 9, 2018
Completion
Jan 9, 2018
Last update
Apr 28, 2020

Study contacts

Julien SEITZ, MD
principal investigator · Hopital saint Joseph

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Apr 2020. You cannot join it, but the record below documents what was studied.

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