DAPREB: DAPERB 3,4-DiAminoPyridine and Electrophysiological Response in Brugada Syndrome

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Terminated
CT.gov ID
NCT00701077
Collaborator
(none)
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2
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Study Details

Study Description

Brief Summary

The Brugada syndrome is a rare disease potentially leading to severe arrhythmic events in otherwise healthy subjects.In many patients an Implantable cardiovertor defibrillator (ICD) is implanted to prevent sudden cardiac death. ICD are however associated with potential complications and are not available in all countries.Pharmacological blockade of specific ion channels (Ito) represents a promising therapeutic approach in this syndrome.The 3,4-diaminopyridine (3,4-DAP) is a pharmacological Ito blocker that can be used in humans.The aim of the study is to evaluate the effect of 3,4-DAP on ventricular arrhythmia inducibility in Brugada patients requiring an electrophysiological study for arrhythmic risk stratification.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

Background:

The Brugada syndrome is a rare disease potentially leading to severe arrhythmic events in otherwise healthy subjects.In many patients an Implantable cardiovertor defibrillator (ICD) is implanted to prevent sudden cardiac death. ICD are however associated with potential complications and are not available in all countries.Pharmacological blockade of specific ion channels (Ito) represents a promising therapeutic approach in this syndrome. Experimental data show that increased Ito current may be associated with both the ECG feature and arrhythmogenic substrate observed in the syndrome. Moreover, Ito blockade reverse the ECG abnormalities and suppress arrhythmogenicity.The 3,4-diaminopyridine (3,4-DAP) is a pharmacological Ito blocker that is already used in humans for another indication.

Main objective:

The aim of the study is to evaluate the effect of 3,4-DAP on ventricular arrhythmia inducibility in Brugada patients requiring an electrophysiological study for arrhythmic risk stratification.

First end point:

Re-inducibility or non re-inducibility of sustained ventricular arrhythmia during electrophysiological study on treatment

Tested hypothesis:

The 3,4-DAP decreases the proportion of re-inducibility during the electrophysiological study with a re-inducibility rate of 80% in the placebo group and 25% in the 3,4-DAP group

Secondary objective:
  • to assess the effect of 3,4-DAP on ST segment elevation in Brugada patients

  • to describe the relationship between 3,4-DAP plasma concentration measured at 45 minutes and electrophysiological study result and ST segment elevation

Study design:

2 centres, randomised, double blind, parallel groups, placebo controlledA single dose of 20 mg of 3,4-DAP

Included patients and number of patients:

Included patients will all have a diagnosed Brugada type 1 ECG and will require an electrophysiological study for arrhythmic risk stratification purpose. Only inducible patients will be included in the study.Using a classical approach, the hypothesis would be that 80% of on placebo patients would be re-inducible when only 25% of on drug patients would. To test such an hypothesis, 32 patients (16 in each group) would have been necessary (a=5%, b=20%).Provided the essential binary response of the electrophysiological study we choose a sequential approach in order to get the opportunity stop for success or futility the inclusions before the end of the study. The maximum number of included patients will then be 42 (21 in each group).

Protocol duration:

Study duration is 48 hours for each patient.The protocol duration is planned for 5 years.

Per protocol procedures:
  • Electrophysiological study with ventricular programmed stimulation performed twice

  • Continuous ECG recording- Blood sampling for 3,4-DAP plasma concentration measurement Potential implications:If the study hypotheses are confirmed it would then be justified to design long term efficacy studies in Brugada patients implanted with an ICD.

Study Design

Study Type:
Interventional
Actual Enrollment :
5 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
DAPERB 3,4-DiAminoPyridine and Electrophysiological Response in Brugada Syndrome
Actual Study Start Date :
Sep 12, 2008
Actual Primary Completion Date :
Mar 1, 2010
Actual Study Completion Date :
Apr 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

3,4-Di-amino-Pyridine : a single 20 mg dosing

Drug: 3,4-Di-amino-Pyridine
a single 20 mg dosing

Placebo Comparator: 2

Drug: placebo
placebo

Outcome Measures

Primary Outcome Measures

  1. Electrophysiological study result (re-inducibility or not) 45 minutes after drug intake [45 minutes after drug intake]

Secondary Outcome Measures

  1. the effect of 3,4-DAP on ST segment elevation in Brugada patients (45 minutes) [at 45 minutes]

  2. the relationship between 3,4-DAP plasma concentration measured at 45 minutes and electrophysiological study result and ST segment elevation [at 45 minutes]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Man or woman ≥ 18 years old

  • Brugada syndrome diagnosed with a type 1 ECG either spontaneous or drug-induced

  • Electrophysiological study indicated for arrhythmic risk stratification purpose

  • Inducibility of a sustained ventricular tachycardia (> 30 seconds) or ventricular fibrillation requiring defibrillation

  • Physical medical examination

  • Signed written informed consent

Exclusion Criteria:
  • Personal or familial history of epilepsy

  • Pregnancy

  • Body weight > 100 kg

  • the need of >1 counter shock for defibrillation

  • Alcohol or cocaine consumption during the protocol

  • Class I (with the exception of local anaesthesia by lidocaine), II, III and IV antiarrhythmic drugs, antidepressant drugs, ATP dependent potassium channel activators, sultopride not stopped for > 7 halve-lives

  • No medical insurance

Contacts and Locations

Locations

Site City State Country Postal Code
1 Lariboisière University Hospital - Cardiology department Paris France 75010

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris

Investigators

  • Principal Investigator: Fabrice EXTRAMIANA, MD, PhD, Lariboisière University Hospital - Cardiology Department

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT00701077
Other Study ID Numbers:
  • P060802
  • EUDRACT 2007-004133-42
First Posted:
Jun 19, 2008
Last Update Posted:
Dec 7, 2020
Last Verified:
Dec 1, 2020
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 7, 2020