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临床试验/NCT02173028
NCT02173028已完成不适用

RESynchronizaTiOn theRapy and bEta-blocker Titration : RESTORE

Giuseppe Ricciardi4 个研究点 分布在 1 个国家目标入组 254 人开始时间: 2013年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
254
试验地点
4
主要终点
Optimal beta-blockers titration due to CRT

研究概览

简要总结

Patients will be treated according to the clinical practice of the participating centers and to the international guidelines for the treatment of heart failure.The present analysis provides a collection of data about the changes to drug therapy after the "Cardiac Resynchronization Therapy" (CRT) procedure , and any signs and symptoms of intolerance to prescribed medications.

详细描述

The treatment of chronic heart failure is currently based on the use of ACE (Angiotensin Converting Enzyme) inhibitors and beta-blockers. Although this therapy is universally accepted up to 10-20% of patients may be intolerant. Moreover, the majority of patients are not treated with the doses that have been shown to be effective in controlled clinical trials. Although it is possible that even low doses of neurohumoral inhibitors are still effective than placebo, a greater benefit can be obtained at maximum doses. Therefore, it is generally recommended that these agents are used at recommended doses found to be effective in controlled studies. There are many reasons for the lack of prescription neurohumoral inhibitors and their use in non-optimal doses. These include both an inadequate clinical management, and low tolerance to drugs. As far as beta-blockers, their poor tolerability has at least two main causes: 1) the effects not related to heart failure (eg, bradycardia, AtrioVentricular (AV) block, bronchial asthma), 2) the acute negative inotropic effects, which can cause a further deterioration of hemodynamic parameters.

The primary objective of the analysis is to demonstrate that cardiac resynchronization therapy (CRT) may allow titration of beta-blockers (carvedilol or bisoprolol) until the optimal dosage, or at least to the effective dose, in patients with heart failure treated to maximal doses of beta-blockers and with the indications for CRT according to current international guidelines.

The secondary objective is to evaluate the effectiveness of remote monitoring with a telemedicine system to facilitate the automatic titration of beta-blockers in comparison with the standard approach, which consists of periodic outpatient visits. The strategy adopted will depend on the availability of remote monitoring systems and standard clinical practice of each participating center.

In addition, we will evaluate the clinical response to CRT, depending on the optimal or sub-optimal dosage of beta-blockers.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

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

入选标准

  • •Patients on optimal therapy for heart failure (diuretics, ACE inhibitors and aldosterone antagonists), with stable dose in the previous month;
  • •Successfully implanted with CRT-D according to current European Society of Cardiology (ESC) guidelines;
  • •New York Heart Association (NYHA) functional class: II, III and IV;
  • •Left Ventricular Ejection Fraction (LVEF) ≤ 35%;
  • •Duration of ventricular depolarization wave (QRS) ≥ 120ms (NYHA III or IV) or ≥ 150ms in NYHA II;
  • •Patients with chronic atrial fibrillation will be eligible for the study only if they undergo ablation ;
  • •18 years or above

排除标准

  • •Failure to comply with the scheduled follow-up;
  • •Life expectancy less than 12 months ;
  • •Pregnant women;
  • •Tricuspid valve mechanics;
  • •Severe aortic stenosis or other valve disease ;
  • •Patients already receiving CRT.

结局指标

主要结局

Optimal beta-blockers titration due to CRT

时间窗: 3 months

The primary objective of the analysis is to demonstrate that cardiac resynchronization therapy (CRT) may allow titration of beta-blockers (carvedilol or bisoprolol) until the optimal dosage, or at least to the effective dose, in patients with heart failure treated to maximal doses of beta-blockers and with the indications for CRT according to current international guidelines.The goal is to achieve the optimal dosage of 10mg/die of bisoprolol or 50mg/die of carvedilol, or at least the recommended dose (carvedilol 37.5 mg / day or bisoprolol 7.5 mg), as shown in international treatment guidelines.

次要结局

  • Beta-blocker Titration with telemedicine system(3 months)
  • Clinical response to CRT(12 months)

研究者

发起方
Giuseppe Ricciardi
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Giuseppe Ricciardi

Principal Investigator

University of Florence

研究点 (4)

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