NCT05508256RecruitingPhase 4
CAtheter-Based Ablation of Atrial Fibrillation Compared to Conventional Treatment in Patients With Heart Failure With Preserved Ejection Fraction
Source: ClinicalTrials.gov · Last updated 6 Mar 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The objective of CABA-HFPEF is to test whether catheter ablation (CA) for atrial fibrillation (AF) can prevent adverse cardiovascular outcomes in patients with heart failure with preserved (HFpEF) or mildly reduced ejection fraction (HFmrEF).
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 4
- Study type
- Interventional
- Enrollment
- 1548 (estimated)
- First submitted
- 10 Aug 2022
- Start date
- 1 Mar 2023
- Primary completion date
- 31 Jul 2026
- Lead sponsor
- Charite University, Berlin, Germany
- Diseases
- Heart failure, Atrial fibrillation
- NCT number
- NCT05508256
What you commit to
- Study type: Interventional · Phase 4
- Planned participants: 1548
- From 1 Mar 2023 to the primary completion date, 31 Jul 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
- Previous left atrial CA or surgical therapy of AF
- Prior heart transplant or listed for heart transplant or cardiac assist device implantation
Other illness
- Valvular heart disease needing interventional or surgical treatment within 3 months
- Heart surgery planned within 3 months
- Any disease that limits life expectancy to less than 1 year
- Active systemic infection (after successful treatment of infection, patients may be enrolled)
Other
- Patient is unable or unwilling to provide infomed consent
- Patient is not suitable for rhythm control of AF
- Acutely decompensated HF, NYHA IV (patients can be enrolled after stabilization)
- Untreated hypothyroidism or hyperthyroidism (after successful treatment of thyroid dysfunction, patients may be enrolled)
- Patient has absolute contra-indication to oral anticoagulation
- Women currently pregnant or breastfeeding or women of childbearing potential without highly effective contraception (PEARL-Index \< 1%)
- Patient is included in another clinical trial
- Inability to comply with the study procedures
Who the study is looking for
- Age ≥18 years
- Signed written informed consent
- Clinical evidence of symptomatic heart failure (NYHA Class II-III)
- Paroxysmal or persistent atrial fibrillation (less than 24 months after first diagnosis, documented at least on one 12-lead ECG)
- Left ventricular ejection fraction (LVEF) 40-49%
- OR
- LVEF ≥ 50% with at least one of the following HFpEF echocardiography findings (any local measurement made during the screening epoch):
- LA enlargement defined by at least 1 of the following: LA width (diameter) ≥3.8 cm or LA length ≥5.0 cm or LA area ≥20 cm2 or LA volume ≥55 ml or LA volume index ≥29 ml/m2
- Left ventricular hypertrophy (septal thickness or posterior wall thickness ≥1.1 cm or relative wall thickness \>0.42)
- Patients with at least 1 of the following:
- HF hospitalization (defined as HF listed as the major reason for hospitalization) within 6 months prior to screening visit and NT-proBNP \>200 pg/ml for patients in sinus rhythm (SR) or \>600 pg/ml for patients in AF at the time of blood sampling
- NT-proBNP \>300 pg/ml for patients in SR or \>900 pg/ml for patients in AF on screening ECG
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 |
|---|---|---|---|
| Charité University Medicine Berlin, Campus Virchow Klinikum Coordinator of this site? Confirm its status | Berlin | Germany | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.