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Cardiology Research Dubrava Prospective Registry (CaRDr)

U

University Hospital Dubrava

Status

Enrolling

Conditions

Atrial Fibrillation
Acute Coronary Syndrome
Arrhythmias, Cardiac
Heart Failure

Treatments

Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,

Study type

Observational

Funder types

Other

Identifiers

NCT06090591
DUH-012017

Details and patient eligibility

About

Cardiology Research Dubrava registry is a prospective, single centre registry including patients with acute coronary syndrome with and without ST segment elevation, patients with heart failure who were prescribed with SGLT-2 inhibitors, patients implanted with TAVI, patients with venous thromboembolism, patients with pulmonary embolism who underwent thromboaspiration procedure, patients implanted with ICD, CRT and conduction system pacing devices, as well as patients with atrial fibrillation who underwent pulmonary vein isolation and are prescribed with long-term anticoagulation therapy.

Full description

Cardiology Research Dubrava registry is a prospective, single centre registry including patients with acute coronary syndrome with and without ST segment elevation, patients with heart failure who were prescribed with SGLT-2 inhibitors, patients implanted with TAVI, patients with venous thromboembolism, patients with pulmonary embolism who underwent thromboaspiration procedure, patients implanted with ICD, CRT and conduction system pacing devices, as well as patients with atrial fibrillation who underwent pulmonary vein isolation and are prescribed with long-term anticoagulation therapy.

In this long-term follow-up registry we plan to collect data on clinical status, standard laboratory results including lipidogram values, NTproBNP values after specific interventions (in.ex. TAVI implantation, SGLT2inh prescripition), bleeding complications, and every major cardiovascular event, including cardiovascular death and all cause death.

Enrollment

3,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: patients implanted with CIED, or with VTE, or with ACS or with TAVI -

Exclusion Criteria: non compliance, not undergoing follow-up at this center

Trial design

3,000 participants in 6 patient groups

Acute coronary syndrome - ACS
Description:
patients who were diagnosed with acute coronary syndrome: STEMI, non-STE ACS - NSTEMI and unstable angina, who underwent coronary angiography and were prescribed with optimal medicament therapy
Treatment:
Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,
Transcatheter aortic valve implantation - TAVI
Description:
patients with aortic stenosis who underwent transcatheter percotaneous implantation of the arteficial aortic valve
Treatment:
Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,
Venous thromboembolism - VTE
Description:
patients with pulmonary embolism and deep vein thrombosis, with a focus on those who underwent thromboaspiration due to high or medium-high risk pulmonary embolism
Treatment:
Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,
Heart failure with SGLT2 inhibitor therapy included - HF-SGLT2
Description:
patients with heart failure with reduced, mid-reduced and preserved systolic function who were prescribed with a SGLT-2 inhibitor therapy, and other optimal medicament therapy for HF
Treatment:
Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,
Cardiac implantable electronic device - CIED
Description:
patients who were implanted with a cardiac implantable electronic device: pacemaker, conduction system pacing device, cardioverter-defibrilator or cardiac resynchronization therapy with or without defibrilator option
Treatment:
Other: SGLT-2 inh therapy, CIED implantation, thromboaspiration,
Arrhythmias
Description:
patients who underwent electrophysiology study, including PVI for atrial fibrillation, as well as SVT ablations, and ventricular arrhythmia ablation (both premature ventriclar beats and ventricular tachycardia ablation in ischsmic and non-ischemic cardiomyopathy).

Trial contacts and locations

1

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Central trial contact

Ivana Jurin, M.D.; Ivan Zeljkovic, M.D.

Data sourced from clinicaltrials.gov

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