NCT07795892Active, not recruiting
Circulating RNA Markers of Ventricular Arrhythmias in Remotely Monitored Patients With Post-Infarction Heart Failure and Implanted Cardioverter-Defibrillators
The Role of Non-Coding RNA Molecules as Potential Markers of Ventricular Arrhythmias in Patients With Post-Myocardial Infarction Heart Failure and Implanted Cardioverter-Defibrillators Undergoing Remote Monitoring
Source: ClinicalTrials.gov · Last updated 31 Aug 2026
Brief summary (registry, in English)
This prospective observational study evaluates whether circulating small non-coding RNAs, particularly microRNAs, are associated with ventricular arrhythmias in patients with post-myocardial infarction heart failure who have an implanted cardioverter-defibrillator and are followed by remote monitoring. Blood samples were collected from 57 participants. Small RNA profiles are analyzed in relation to ventricular tachycardia or ventricular fibrillation episodes recorded by the implanted device. Participants are not assigned to any treatment or intervention as part of this study. The initial analysis includes six months of follow-up, with longer-term observational follow-up planned.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 57 (actual)
- First submitted
- 26 Aug 2026
- Start date
- 12 Mar 2026
- Primary completion date
- 12 Sept 2026
- Lead sponsor
- University of Rzeszow
- Diseases
- Heart failure
- NCT number
- NCT07795892
What you commit to
- Study type: Observational
- Participants enrolled: 57
- From 12 Mar 2026 to the primary completion date, 12 Sept 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Concurrent participation in another study evaluating a drug or therapeutic intervention
Age
- Age younger than 18 years
Other
- Lack of informed consent or withdrawal of consent
Who the study is looking for
- Age 18 years or older
- Post-myocardial infarction heart failure
- Previous implantation of an implantable cardioverter-defibrillator or cardiac resynchronization therapy defibrillator
- Participation in a remote monitoring program for the implanted device
- Written informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Clinical Provincial Hospital No. 2 in Rzeszow Coordinator of this site? Confirm its status | Rzeszów | Poland | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.