- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01254474
Evaluation of Depolarization and Repolarisation Activity During Cardiac Arrhythmia Using a Novel Monophasic Action Potential Catheter (EvaMAP)
Monophasic action potential (MAP) recording plays an important role in a more direct view of human myocardial electrophysiology under both physiological and pathological conditions. The MAP method represents a very useful tool for an electrophysiological research in cardiology. Its crucial importance lies in the fact that it enables the study of the action potential (AP) of myocardial cell in vivo and, therefore, the study of the dynamic relation of this potential with all the organism variables what can be particularly helpful in the case of arrhythmias.
Hundred and fifty patients will be included to explore mapping capabilities in cardiac chambers in patients suffering from regular or fibrillating tachycardia's with the following inclusion plan: i) Atrial fibrillation at a total of 50 patients ii) Ventricular fibrillation or patients at high risk of sudden cardiac death at a total of 50 patients iii) Junctional tachycardia at a total of 50 patients. We will focus on cardiac activation (depolarization and repolarization) in this population.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Pessac, France, 33604
- Hôpital cardiologique du Haut-Lévêque, Cardiac arrhythmias department
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patients with Atrial Fibrillation or Ventricular Fibrillation or junctional tachycardia or reentrant tachycardia
- Age ≥ 18 years old
- Signed patient informed consent form
- Affiliated to social security (European countries)
Exclusion Criteria:
- Patients under 18 years old
- Pregnancy
- Psychiatric disorders
- Neurological sequelae after a prior cardiac arrest that prevents informed consent
- Absence of informed consent form
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: MAP 4 procedure
Assess MAP 4 mapping capabilities in cardiac chambers in patients suffering from regular or fibrillating tachycardia's
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cardiac activation identified during the intervention by depolarization and repolarization times
Time Frame: End of mapping procedure (up to 5 days after inclusion)
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The performance criteria of this MAP4 catheter will be evaluated in providing information on the action potentials to further improve insight into mechanisms. Cardiac activation (depolarization and repolarization) identified during the intervention with established criteria:
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End of mapping procedure (up to 5 days after inclusion)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Presence of zone of low voltage (<0.5 mV)
Time Frame: End of mapping procedure (up to 5 days after inclusion)
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End of mapping procedure (up to 5 days after inclusion)
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|
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Presence of post depolarization on MAP4 catheter
Time Frame: End of mapping procedure (up to 5 days after inclusion)
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End of mapping procedure (up to 5 days after inclusion)
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Adverse events during procedure and/or during 6 months
Time Frame: 6 months
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6 months
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Skin to skin procedural time
Time Frame: End of mapping procedure (up to 5 days after inclusion)
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Skin to skin procedural time (major reduction of time mapping is expected with MAP4.
This variable is appreciated by the duration of the procedure and fluoroscopic time (in minutes))
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End of mapping procedure (up to 5 days after inclusion)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Mélèze HOCINI, MD, University Hospital Bordeaux, France
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- CHUBX 2010/42
- 2010-A00967-32 (Other Identifier: ANSM)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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