Actively Recruiting
Syncope-Asystole Latency Time in Tilt Table Test: The SALT-TILT Study
Led by Azienda Ospedaliera di Bolzano · Updated on 2024-04-11
64
Participants Needed
1
Research Sites
153 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Syncope is a common presenting condition. Pacemaker implantation can significantly reduce syncope recurrences in reflex syncope. However, despite careful selection, a substantial proportion of patients treated with pacemakers suffer recurrences of syncope. It is thought that a pronounced vasodepressor component may hinder the efficacy of pacing in patients, preventing adequate cerebral perfusion during the reflex, thus relativizing the anti-bradycardia function of the pacemaker to prevent syncope. It is hypothesised that the time elapsed from the actual loss of consciousness to the asystole recorded on the ECG during Tilt Table Test may be predictive in terms of response to pacemaker therapy, so this parameter becomes the subject of the present study.
CONDITIONS
Official Title
Syncope-Asystole Latency Time in Tilt Table Test: The SALT-TILT Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients eligible for invasive treatment according to the ESC Guidelines for pacing 2021
- Written informed consent
You will not qualify if you...
- Other condition which explains syncope cause other than reflex syncope
- Structural heart disease (valvular, ischaemic, cardiomyopathies)
- Pregnancy
- Patient denial to be recorded on video during tilt table test
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Azienda Sanitaria di Bolzano
Bolzano, Italy, 39100
Actively Recruiting
Research Team
M
Matthias Unterhuber, Dr. Dr.
CONTACT
M
Marco Tomaino, Dr.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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