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NCT07521800Recruiting

Remote ECG Monitoring Post TAVI

Remote ECG Monitoring as a Diagnostic Tool for Therapeutic Strategies After Transcatheter Aortic Valve Replacement: Rationale and Design of the DRAGON-TAVI Trial.

Source: ClinicalTrials.gov · Last updated 13 Apr 2026

Brief summary (registry, in English)

The DRAGON TAVI study is a multicenter, prospective, open, randomised trial, which will enrol 250 patients, randomized 1:1 to the study group (continuous 30-day ECG monitoring with visits triggered by ECG findings) and standard care (ie. control group, which will receive the standard post op 24-48h ECG monitoring and a regular follow-up visit with standard ECG within 30 days). The duration of the study is 12 months ± 1 month.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
250 (estimated)
First submitted
24 Nov 2025
Start date
Dec 2023
Primary completion date
Feb 2027
Lead sponsor
Medical University of Silesia
NCT number
NCT07521800

What you commit to

  • Study type: Interventional
  • Planned participants: 250
  • From Dec 2023 to the primary completion date, Feb 2027
  • 4 sites in 2 countries
  • 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

  • Previously known conduction disturbances\*\*
  • Ischaemic stroke, TIA, MI or heart surgery within 1 month before TAVI qualification
  • Chronic immunosuppressive therapy

Other illness

  • History of atrial fibrillation or atrial flutter
  • Haemorrhagic stroke within 1 year before TAVI qualification
  • Comorbidities (e.g. drug addiction, alcohol abuse, emotional/mental disorders) which do not allow safe participation in the study

Other

  • Presence of: pacemaker, CRT-P, ICD, CRT-D before or after TAVI

Who the study is looking for

  • Patient age over 18 years old
  • Severe aortic stenosis
  • Moderate or high cardiovascular risk based on current ESC Guidelines "Heart Team" qualification for TAVI
  • Written informed consent of the patient for 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
Division of Cardiology, Departement of Medical Science University of Turin, Città della Salute e Della Scienza
Coordinator of this site? Confirm its status
TurinItalyRecruiting
Department of Invasive Cardiology, Medical University of Białystok, Bialystok, Poland
Coordinator of this site? Confirm its status
BialystokPolandRecruiting
Department of Cardiology and Structural Heart Diseases, Medical University of Silesia, Katowice, Poland
Coordinator of this site? Confirm its status
KatowicePolandNot yet recruiting
Medical University of Silesia
Coordinator of this site? Confirm its status
KatowicePolandRecruiting

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