Syncope-Asystole Latency Time in Tilt Table Test: The SALT-TILT Study
NCT ID: NCT06356207
Last Updated: 2024-04-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
64 participants
OBSERVATIONAL
2024-03-20
2027-03-31
Brief Summary
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Detailed Description
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The main target of the study is to evaluate the time elapsed between the T-LOC during Video Tilt Table Testing and the asystole at the ECG using a registry and to assess its predictive value in patients undergoing invasive treatment. The hypothesis is that a vasodepressive component could lessen the effect of pacing in a patient, leading to cerebral hypoperfusion and syncope despite maintaining a stable rhythm.
This is a prospective, multi-center observational study with 2 year follow-up of patients. Patients eligible for invasive treatment of reflex syncope are included.
If after guideline-directed implantable loop recorder insertion no cardioinhibition has been recorded, the patient is included automatically in the registry.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients affected by neuronally mediated syncope
Tilt Table Test
The main goal of the study is to evaluate the time elapsed between the T-LOC during Video Tilt Table Testing and the asystole at the ECG using a national registry and to assess its predictive value in patients undergoing invasive treatment. The hypothesis is that a vasodepressive component could lessen the effect of pacing in a patient, leading to cerebral hypoperfusion and syncope despite maintaining a stable rhythm.
Interventions
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Tilt Table Test
The main goal of the study is to evaluate the time elapsed between the T-LOC during Video Tilt Table Testing and the asystole at the ECG using a national registry and to assess its predictive value in patients undergoing invasive treatment. The hypothesis is that a vasodepressive component could lessen the effect of pacing in a patient, leading to cerebral hypoperfusion and syncope despite maintaining a stable rhythm.
Eligibility Criteria
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Inclusion Criteria
* Written informed consent
Exclusion Criteria
* Structural heart disease (valvular, ischaemic, cardiomyopathies)
* Pregnancy
* Patient denial to be recorded on video during tilt table test
18 Years
ALL
No
Sponsors
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Azienda Ospedaliera di Bolzano
OTHER
Responsible Party
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Matthias Unterhuber
Principal Investigator
Locations
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Azienda Sanitaria di Bolzano
Bolzano, , Italy
Countries
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Central Contacts
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Facility Contacts
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Marco Tomaino, Dr.
Role: primary
Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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113-2023
Identifier Type: -
Identifier Source: org_study_id
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