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Effect of Closed Loop Pacemaker Treatment on Recurrent Vasovagal Syncope

Primary Purpose

Vasovagal Syncope

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Pacemaker treatment, pacemaker programmed as active = CLS
Pacemaker, programmed as passive = VVI 30 beats per minute (bpm)
Sponsored by
Aarhus University Hospital Skejby
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vasovagal Syncope focused on measuring vasovagal syncope, syncope, cardioinhibitory syncope, neurocardiogenic syncope, pacing, closed loop pacing, tilt table

Eligibility Criteria

25 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: A clinical problem with vasovagal syncope which motivates considerations concerning pacemaker treatment. A positive tilt-table test. Exclusion of other causes for syncope by a complete diagnostic work-up allowing only minor cardiac abnormalities Syncope for >= 2 years. Number of syncopal episodes >= 3 At least 1 instance of syncope within the last 6 months. A positive tilt-table test which reproduces the clinical syncope and is associated with a clearly abnormal haemodynamic response: Vasovagal Syncope International Study (VASIS) type 1 with bradycardia < 40 bpm, or VASIS type 2A, or VASIS type 2B Stable clinical condition Able to accept and follow the protocol and give written consent. Exclusion Criteria: Conventional indication for pacemaker (i.e. atrioventricular [AV] block) Indication for cardiac resynchronisation therapy (i.e. left bundle branch block [LBBB]) Documented atrial fibrillation or flutter Epilepsy Congestive heart failure History of myocardial infarction (MI) or angina pectoris Serious chronic disease, life expectancy < 3 years. Age < 25 years Pregnant and lactating women Participating in other investigation

Sites / Locations

  • Henning Mølgaard, MD, DMSc

Outcomes

Primary Outcome Measures

Recurrence of syncope, active (CLS pacing) versus passive (VVI=30) pacing period

Secondary Outcome Measures

Number of syncopal and presyncopal episodes, active versus passive pacing period
Quality of life, active versus passive pacing period

Full Information

First Posted
February 15, 2006
Last Updated
March 31, 2010
Sponsor
Aarhus University Hospital Skejby
Collaborators
Aarhus University Hospital, Biotronik SE & Co. KG
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1. Study Identification

Unique Protocol Identification Number
NCT00292825
Brief Title
Effect of Closed Loop Pacemaker Treatment on Recurrent Vasovagal Syncope
Official Title
SCANdinavian Vasovagal SYNCope Pacemaker Investigation (SCANSYNC)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
March 2010 (Actual)
Study Completion Date
March 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Aarhus University Hospital Skejby
Collaborators
Aarhus University Hospital, Biotronik SE & Co. KG

4. Oversight

5. Study Description

Brief Summary
The main purpose is to prevent syncope in patients with recurrent syncopal episodes caused by malignant vasovagal faints and bradycardia. Patients are treated by a special pacemaker (closed loop stimulation [CLS]) which can potentially identify an incipient attack and prevent syncope by pacing.
Detailed Description
The treatment of patients with recurrent syncope of vasovagal origin, not precipitated by usual vasovagal factors, and not associated with structural heart disease, is unsolved. The limitations of the conducted 5 pacemaker studies are a significant placebo effect of pacemaker treatment, underpowering and lack of double blinding. The pacemaker intervention has been accelerated dual chamber pacing at the time of bradycardia, which may be too late. However, a pooling of all data indicate a beneficial effect of pacing. Vasodilatation is an obligate element of all vasovagal syncopal episodes and in many also an early sign associated with the hyperkinetic empty left ventricle which triggers the reflex wave. The principle in closed loop stimulation (CLS) is a continuous surveillance of the impedance in the right ventricle which correlates highly with myocardial contractility. When contractility is increased significantly atrial pacing with prolonged AV delay is commenced. This principle has been used in chronotropic incompetent patients and in one small study of patients with vasovagal syncope with a positive outcome. The hypothesis is that the CLS will potentially identify an incipient vasovagal attack and be able to prevent the drop in cardiac output and bradycardia by early accelerated pacing. Patients will be treated 12 months with active pacing (CLS) and then crossed over to 12 months with passive pacing (VVI, 30 bpm). The study will be double blinded, only a technician will know the status of the pacemaker.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vasovagal Syncope
Keywords
vasovagal syncope, syncope, cardioinhibitory syncope, neurocardiogenic syncope, pacing, closed loop pacing, tilt table

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Pacemaker treatment, pacemaker programmed as active = CLS
Intervention Description
Pacemaker treatment with closed loop function(CLS)
Intervention Type
Device
Intervention Name(s)
Pacemaker, programmed as passive = VVI 30 beats per minute (bpm)
Intervention Description
pacemaker treatment as VVI 30 bpm
Primary Outcome Measure Information:
Title
Recurrence of syncope, active (CLS pacing) versus passive (VVI=30) pacing period
Time Frame
12 months + 12 months
Secondary Outcome Measure Information:
Title
Number of syncopal and presyncopal episodes, active versus passive pacing period
Time Frame
12 months+12 months
Title
Quality of life, active versus passive pacing period
Time Frame
12 months+12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A clinical problem with vasovagal syncope which motivates considerations concerning pacemaker treatment. A positive tilt-table test. Exclusion of other causes for syncope by a complete diagnostic work-up allowing only minor cardiac abnormalities Syncope for >= 2 years. Number of syncopal episodes >= 3 At least 1 instance of syncope within the last 6 months. A positive tilt-table test which reproduces the clinical syncope and is associated with a clearly abnormal haemodynamic response: Vasovagal Syncope International Study (VASIS) type 1 with bradycardia < 40 bpm, or VASIS type 2A, or VASIS type 2B Stable clinical condition Able to accept and follow the protocol and give written consent. Exclusion Criteria: Conventional indication for pacemaker (i.e. atrioventricular [AV] block) Indication for cardiac resynchronisation therapy (i.e. left bundle branch block [LBBB]) Documented atrial fibrillation or flutter Epilepsy Congestive heart failure History of myocardial infarction (MI) or angina pectoris Serious chronic disease, life expectancy < 3 years. Age < 25 years Pregnant and lactating women Participating in other investigation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Henning Mølgaard, MD, DMSc
Organizational Affiliation
Department of Cardiology, Skejby Sygehus, Aarhus University Hospital, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Henning Mølgaard, MD, DMSc
City
Århus N
ZIP/Postal Code
8200
Country
Denmark

12. IPD Sharing Statement

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Effect of Closed Loop Pacemaker Treatment on Recurrent Vasovagal Syncope

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