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临床试验/NCT04987723
NCT04987723已完成不适用

A Mechanistic Exploratory Study of AF-induced Cardiac Dysfunction and Symptoms

Barts & The London NHS Trust2 个研究点 分布在 1 个国家目标入组 106 人开始时间: 2022年1月21日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
106
试验地点
2
主要终点
Correlation co-efficient of HRV measures with change in cardiac function

研究概览

简要总结

Although the heart rhythm disorder Atrial Fibrillation (AF) affects 2% of the population, the impact it has on an effected individual can be highly variable. Some people are asymptomatic whilst others can experience debilitating symptoms or heart failure (HF)- weakness of the heart muscle. The reason why this variability exists in unknown and how AF actually drives HF is unclear. HF can also be caused by many other reasons and it can be difficult to identify those patients with HF caused by AF versus patients with AF but their HF is due to a different reason. This is important as it would help us to identify those patients most likely to improve their heart function after the treatment of AF and thus gain more from invasive treatments like AF catheter ablation; which is effective at restoring normal heart rhythm but has some risks attached.

The investigators suspect the characteristics of the AF, such as how irregularly it makes the heartbeat, can be used to predict who will respond better. Studies of heart cells in the lab as well as animal models have suggested this characteristic may be the cause of AF-induced heart muscle weakness and reduce cardiac output, making it a potential predictor that can be measured. Other potential predictors will be measured during pre-procedural scans and tests too. The investigators will also explore whether there are predictors of which patients gain the most symptomatic benefit and gain insight into why some people develop symptoms of AF, whereas others do not.

By studying the structural and functional sequelae of catheter ablation in patients with HF the investigators hope to better understand the relationship between the two diseases.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Referred for first AFCA procedure by their responsible physician.
  • Persistent AF captured on ECG but not in continuous AF for more than 3 years. (Persistent AF will be defined as any continuous episode lasting longer than 7 days or requiring intervention to restore sinus rhythm after this time.)
  • Participants must have either:
  • Left Ventricular Ejection Fraction (LVEF) < 50% by echocardiogram during routine screening or within 12 months prior to enrolment day. The echo must have been performed >3 weeks after optimisation of HF and rate control therapies, otherwise repeat imaging will be performed after this has been achieved
  • o NYHA functional status II-III at the enrolment visit.
  • o Left Ventricular Ejection Fraction (LVEF) >50% by echocardiogram during routine screening or within 12 months prior to enrolment day.
  • o modified European Heart Rhythm Association 2a-4.

排除标准

  • Previous left atrial ablation procedure or surgery.
  • Contraindication to chronic anticoagulation therapy or heparin
  • Unable or unwilling to consent to investigation and follow-up requirements or inability to comply with planned study procedures.
  • LA anteroposterior diameter ≥ 5.5 cm or indexed LA volume ≥ 50mL/m2 on echo.
  • Recent (last 6 months) event that may impact LV function- myocardial infarction, coronary revascularization, pacemaker or cardiac resynchronization therapy.
  • AF suspected to be due to a reversible cause (e.g. hyperthyroidism, recent surgery)
  • Acute coronary syndrome within 4 weeks as defined by ECG ST segment depression or prominent T-wave inversion and/or positive biomarkers of necrosis (e.g. troponin) in the absence of ST-segment elevation and in an appropriate clinical setting (chest discomfort or angina equivalent).
  • Cardiac surgery, angioplasty, or cerebrovascular accident within 4 weeks prior to enrolment.
  • Life expectancy less than 1 year.
  • Chronic kidney disease stage 4 or
  • Any of the below cardiac diagnoses:
  • Hypertrophic obstructive cardiomyopathy
  • Severe valvular disease
  • Restrictive or constrictive cardiomyopathy, including known amyloidosis, sarcoidosis,
  • haemochromatosis
  • Complex congenital heart disease
  • Constrictive pericarditis
  • Severe pulmonary hypertension (RVSP > 60 mmHg),
  • Non-cardiac pulmonary oedema
  • Active myocarditis

研究组 & 干预措施

AF + symptoms cohort

Other

Left Ventricular Ejection Fraction (LVEF) > 50% by echocardiogram during routine screening or within 12 months prior to enrolment day

With

modified European Heart Rhythm Association symptom classification 2b-4.

干预措施: Patient questionnaires (Other)

AF + HFrEF cohort

Other

Left Ventricular Ejection Fraction (LVEF) < 50% by echocardiogram during routine screening or within 12 months prior to enrolment day. The echo must have been performed >3 weeks after optimisation of HF and rate control therapies, otherwise repeat imaging will be performed after this has been achieved

With

NYHA functional status II-III at the enrolment visit.

干预措施: Holter monitoring (Other)

AF + HFrEF cohort

Other

Left Ventricular Ejection Fraction (LVEF) < 50% by echocardiogram during routine screening or within 12 months prior to enrolment day. The echo must have been performed >3 weeks after optimisation of HF and rate control therapies, otherwise repeat imaging will be performed after this has been achieved

With

NYHA functional status II-III at the enrolment visit.

干预措施: stress echocardiography (Other)

AF + HFrEF cohort

Other

Left Ventricular Ejection Fraction (LVEF) < 50% by echocardiogram during routine screening or within 12 months prior to enrolment day. The echo must have been performed >3 weeks after optimisation of HF and rate control therapies, otherwise repeat imaging will be performed after this has been achieved

With

NYHA functional status II-III at the enrolment visit.

干预措施: Cardiac MRI (Other)

AF + HFrEF cohort

Other

Left Ventricular Ejection Fraction (LVEF) < 50% by echocardiogram during routine screening or within 12 months prior to enrolment day. The echo must have been performed >3 weeks after optimisation of HF and rate control therapies, otherwise repeat imaging will be performed after this has been achieved

With

NYHA functional status II-III at the enrolment visit.

干预措施: Patient questionnaires (Other)

AF + symptoms cohort

Other

Left Ventricular Ejection Fraction (LVEF) > 50% by echocardiogram during routine screening or within 12 months prior to enrolment day

With

modified European Heart Rhythm Association symptom classification 2b-4.

干预措施: Holter monitoring (Other)

结局指标

主要结局

Correlation co-efficient of HRV measures with change in cardiac function

时间窗: 6 months after catheter ablation

This will be calculated in the AF + HFreF arm Cardiac function will be measured as three endpoints: * LVEF on echocardiography * Serum NT-proBNP * VO2 peak on CPET

次要结局

  • Correlation co-efficient of LA strain with change in cardiac function(6 months after catheter ablation)
  • Correlation co-efficient of HRV measures with change in score on validated AF PROM questionnaire(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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