Observational registry for patients with left bundle branch block
Registro Osservazionale Dei Pazienti Con Blocco Della Branca Sinistra
Azienda Ospedaliero Universitaria di Sassari · NCT05283603
This study looks at patients with left bundle branch block to see how it affects their heart function and overall health, using different tests to gather important information for better treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 1000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Azienda Ospedaliero Universitaria di Sassari (other) |
| Locations | 1 site (Sassari) |
| Trial ID | NCT05283603 on ClinicalTrials.gov |
What this trial studies
This observational registry aims to investigate the clinical and imaging features of patients diagnosed with left bundle branch block (LBBB) on ECG. It will analyze a large cohort to identify predictors of LBBB-induced left ventricular systolic dysfunction and overall patient outcomes. The study will utilize various diagnostic tools, including ECG, echocardiograms, and magnetic resonance imaging, to gather comprehensive data that may influence future therapeutic management of these patients.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who have been diagnosed with left bundle branch block on their ECG.
Not a fit: Patients with previous extensive anterior myocardial infarction, cardiac surgery, congenital heart disease, or those with permanent pacing devices may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and management of heart failure in patients with LBBB.
How similar studies have performed: While there may be studies on LBBB, this specific observational approach focusing on predictors of dysfunction is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * LBBB on ECG Exclusion Criteria: * Previous extensive anterior myocardial infarction * Previous cardiac surgery or transcatheter aortic valve implantation (TAVI) * Congenital structural heart disease * Patients implanted with permanent right ventricular stimulation devices and permanent pacing * Denial to consent
Where this trial is running
Sassari
- Cardiology, AOU Sassari — Sassari, Italy (RECRUITING)
Study contacts
- Study coordinator: Giuseppe D Sanna, MD PhD
- Email: giuseppe.sanna@aousassari.it
- Phone: +39 0792061561
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Left Bundle Branch Block on ECG