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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
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

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Albacete University Hospital Complex
Coordinator of this site? Confirm its status
AlbaceteSpainNot yet recruiting
Ciudad Real General University Hospital
Coordinator of this site? Confirm its status
Ciudad RealSpainRecruiting
12 de Octubre University Hospital
Coordinator of this site? Confirm its status
MadridSpainRecruiting
Ramón y Cajal University Hospital
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting

This page is information, not medical advice. Discuss any trial with your doctor.