Wolff-Parkinson-White Syndrome Anterograde Refractory Period of Accessory Duct
Not Applicable
Terminated
- Conditions
- Wolff-Parkinson-White Syndrome
- Interventions
- Procedure: esophagal stimulation
- Registration Number
- NCT00873470
- Lead Sponsor
- Nantes University Hospital
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 13
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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Stimulation esophagal stimulation All patients included have the stimulation
- Primary Outcome Measures
Name Time Method Measurement of effective anterograde refractory period of accessory duct and its evolution for a follow up superior to 10 years Day 0
- Secondary Outcome Measures
Name Time Method Triggering a supra-ventricular tachycardia during the stimulation. Day 0 Presence of symptoms linked to WPW syndrome during the interval separating the 2 esophageal stimulation. Day 0
Trial Locations
- Locations (1)
Nantes UH
🇫🇷Nantes, France