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Wolff-Parkinson-White Syndrome Anterograde Refractory Period of Accessory Duct (WPW)
This study is currently recruiting participants.
Verified by Nantes University Hospital, March 2009
First Received: March 31, 2009   No Changes Posted
Sponsored by: Nantes University Hospital
Information provided by: Nantes University Hospital
ClinicalTrials.gov Identifier: NCT00873470
  Purpose

The study consists of the realization of a new esophageal stimulation for patients already stimulated 10 years ago. The investigators would like to make a long term evaluation of the evolution of anterograde effective refractory period of accessory duct in the WPW syndrome. This study will be realized by esophageal stimulation.


Condition Intervention
Wolff-Parkinson-White Syndrome
Procedure: esophagal stimulation

Study Type: Interventional
Study Design: Open Label, Uncontrolled, Single Group Assignment
Official Title: Long Term Evolution of the Anterograde Refractory Period of Accessory Duct in the Wolff-Parkinson-White Syndrome

Resource links provided by NLM:


Further study details as provided by Nantes University Hospital:

Primary Outcome Measures:
  • Measurement of effective anterograde refractory period of accessory duct and its evolution for a follow up superior to 10 years [ Time Frame: Day 0 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Triggering a supra-ventricular tachycardia during the stimulation. [ Time Frame: Day 0 ] [ Designated as safety issue: No ]
  • Presence of symptoms linked to WPW syndrome during the interval separating the 2 esophageal stimulation. [ Time Frame: Day 0 ] [ Designated as safety issue: No ]

Estimated Enrollment: 33
Study Start Date: February 2009
Estimated Study Completion Date: February 2010
Estimated Primary Completion Date: February 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Stimulation: Experimental
All patients included have the stimulation
Procedure: esophagal stimulation
ECG (rest) esophagal stimulation (rest and during effort)

  Eligibility

Ages Eligible for Study:   21 Years to 64 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 21 < age < 64 years
  • First esophagal stimulation with evaluation of effective anterograde refractory period > 10 years
  • Informed consent signed
  • Diagnosis of Wolff-Parkinson-White syndrome
  • No procedure of ablation of accessory duct

Exclusion Criteria:

  • Ablation of accessory duct
  • Patient with contraindication to esophageal stimulation
  • Patient with contraindication to effort test
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00873470

Contacts
Contact: Gilles Lande, MD 06 15 40 83 92 gilles.lande@chu-nantes.fr

Locations
France
Nantes UH Recruiting
Nantes, France, 44093
Contact: Gilles Lande, MD     06 15 40 83 92     gilles.lande@chu-nantes.fr    
Principal Investigator: Gilles Lande, MD            
Sponsors and Collaborators
Nantes University Hospital
  More Information

No publications provided

Responsible Party: Nantes UH ( Anne Omnes )
Study ID Numbers: BRD 08/9-I
Study First Received: March 31, 2009
Last Updated: March 31, 2009
ClinicalTrials.gov Identifier: NCT00873470     History of Changes
Health Authority: France: Afssaps - French Health Products Safety Agency

Study placed in the following topic categories:
Wolff-Parkinson-White Syndrome
Ganglion Cysts
Heart Diseases
Cardiovascular Abnormalities
Basal Ganglia Diseases
Central Nervous System Diseases
Brain Diseases
Neurodegenerative Diseases
Parkinson Disease
Movement Disorders
Parkinsonian Disorders
Congenital Abnormalities
Heart Defects, Congenital
Pre-Excitation Syndromes
Arrhythmias, Cardiac

Additional relevant MeSH terms:
Wolff-Parkinson-White Syndrome
Heart Diseases
Disease
Cardiovascular Abnormalities
Basal Ganglia Diseases
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Neurodegenerative Diseases
Pathologic Processes
Parkinson Disease
Movement Disorders
Syndrome
Cardiovascular Diseases
Parkinsonian Disorders
Congenital Abnormalities
Heart Defects, Congenital
Arrhythmias, Cardiac
Pre-Excitation Syndromes

ClinicalTrials.gov processed this record on September 02, 2009