Assesment of the Clinical Benefit of Provocation on Tilt-table in SYNCope Patients, TiltSYNC-trial

ConditionVasovagal Syncope (VVS)

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

About this trial

multicenter prospective randomized controlled comparison of biofeedback with tilt table testing (investigational management strategy) vs biofeedback without tilt table testing (reference management strategy) in patients with certain/highly likely vasovagal syncope

Eligibility criteria

Qualifiers

All patients >18 years of age with certain/highly likely vasovagal syncope after the guideline based syncope evaluation

Disqualifiers

Those aged <18 years

Any patient diagnosed with another form of reflex syncope other than vasovagal syn-cope

Contraindication for tilt table testing at the discretion of the responsible physician

Those with a learning disability

Trial design

Treatments tested in this trial

biofeedback and standard of care with tilt table testing
no tilt table testing

Treatment groups

238 Participants

are divided into 2 treatment groups

Sponsors and collaborators

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Lead sponsor

Source ClinicalTrials.gov