NCT06896266Recruiting
Genetic Characterization of Patients With Arrhythmia-Induced Cardiomyopathy
Understanding and Characterizing the Genetics of Patients With Arrhythmia-Induced Cardiomyopathy
Source: ClinicalTrials.gov · Last updated 15 Sept 2026
Brief summary (registry, in English)
The goal of this observational study is to learn about the genetic insights of arrhythmya-induced cardiomyopathy and its clinical prognosis. The main questions it aims to answer are: I. Does patients with arrhythmia-induced cardiomyopathy have a greater proportion of genetic mutations compared with other types of cardiomyopathy or general population? II. Have the genetics any prognostic impact in patients with arrhythmia-induced cardiomyopathy?
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 109 (estimated)
- First submitted
- 13 Mar 2025
- Start date
- 1 Dec 2024
- Primary completion date
- Aug 2027
- Lead sponsor
- Hospital Universitario 12 de Octubre
- Diseases
- Heart failure, Atrial fibrillation
- NCT number
- NCT06896266
What you commit to
- Study type: Observational
- Planned participants: 109
- From 1 Dec 2024 to the primary completion date, Aug 2027
- 4 sites 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
- Presence of known factors causing systolic ventricular dysfunction:
- Prior cardiomyopathy diagnosis.
- Severe mitral or aortic valve disease.
- Non-revascularizable ischemic heart disease.
- Context of peri-resuscitation cardiopulmonary care.
- Abusive alcohol consumption, defined as \>80 grams of ethanol or \>7 standard alcoholic beverages per day.
- Active treatment with chemotherapeutic agents or radiation therapy to the thorax.
- Known infection with Trypanosoma cruzi, Borrellia burgdorferi or other infectious agent causing cardiomyopathy.
Age
- Age \<18 years.
Other
- Refusal of informed consent.
- Legal or juridical incapacity.
- Life expectancy less than 1 year.
- Impossibility of a follow-up of at least 6 months.
- Presence of a ventricular rate \>140 beats per minute, limiting the validity of imaging measurements.
Who the study is looking for
- Presence of atrial fibrillation or atrial flutter not self-limited.
- Performance of a cardiac imaging test with systolic function analysis (echocardiogram, magnetic resonance, CT scan) during the clinical course of the arrhythmia, exhibiting a left ventricular ejection fraction (LVEF) \<50%. In order for the test to be representative, the maximum time between the performance of the imaging test and the rhythm control procedure will be 3 months, in the absence of intervening cardiovascular events that may have caused a variation in LVEF. In the event that the patient had a previously known LVEF \<50%, the change with respect to this attributable to tachyarrhythmia has to be ≥10%.
- Signature of informed consent.
- Ability to understand and accept participation in the study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Albacete University Hospital Complex Coordinator of this site? Confirm its status | Albacete | Spain | Not yet recruiting |
| Ciudad Real General University Hospital Coordinator of this site? Confirm its status | Ciudad Real | Spain | Recruiting |
| 12 de Octubre University Hospital Coordinator of this site? Confirm its status | Madrid | Spain | Recruiting |
| Ramón y Cajal University Hospital Coordinator of this site? Confirm its status | Madrid | Spain | Active, not recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.