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临床试验/NCT03053843
NCT03053843Unknown不适用

Randomized Trial of Mediterranean Diet Plus Extravirgin Olive Oil in the Prevention of Recurrent Arrhythmias. The PREDIMAR (PREvención Con DIeta Mediterránea de Arritmias Recurrentes) Trial

Fundación de investigación HM4 个研究点 分布在 1 个国家目标入组 720 人开始时间: 2017年3月22日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
720
试验地点
4
主要终点
atrial tachyarrhythmias documented by electrocardiogram or recorder device

研究概览

简要总结

Background: Atrial fibrillation (AF) is the most frequent cardiac arrhythmia and represents a high priority public health problem, as in a few decades it will become a possibly unsustainable load for the national health system. Preventive and therapeutic strategies based on the best possible scientific evidence are required. Ablation therapy, despite being the most effective approach, is associated with a 30-35% arrhythmic recurrence rate. An intervention with Mediterranean diet and extra virgin olive oil (EVOO) has proven effective in primary prevention and reduced the incidence of AF in high-risk subjects in a recent, large, randomized trial (PREDIMED).

Methods: Parallel, randomized, multicenter nutritional intervention trial in 640 patients with AF treated with catheter ablation. Two groups will be randomized in a 1:1 ratio: 1) intervention with Mediterranean diet and EVOO; 2) usual care (control group). The primary objective will be the incidence of atrial tachyarrhythmias for two years after ablation. At least 190 recurrences are expected after 2 years (median) of follow-up. A relative risk of 0.7 is assumed and statistical power of 80%. Follow-up visits will be scheduled at 3, 6, 12, 18 and 24 months. In addition to the in-person visits, event monitors will be used to document episodes. Dietary intervention will be carried out by nutritionists who will use methods adapted from the PREDIMED trial with contacts every 2 months. 1 liter of EVOO per week will be provided for free in the intervention arm. Inflammatory markers will be analyzed in both groups during follow-up. Cox models will be used to estimate adjusted hazard ratios.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with symptomatic paroxysmal AF (with evidence of more than one symptomatic episode in the last year and at least one documented episode) upon whom catheter ablation is performed.
  • Patients with persistent symptomatic AF upon whom catheter ablation is performed.

排除标准

  • Serious medical condition that prevents dietary intervention (gastrointestinal disease with intolerance to fats, advanced malignancy, neurological, psychiatric or severe endocrine disease)
  • Any other pathology or medical condition that limits survival to less than one year; Immunodeficiency or HIV-positive,
  • Consumption of illegal drugs,
  • Chronic alcoholism or total consumption of alcohol >80 g/d
  • Body mass index > 40 kg/m 2,
  • Difficulty or major inconvenience with changing dietary habits, inability to follow a style of Mediterranean diet, low probability of changing dietary habits according to the models of Prochaska and Diciemente (Nigg, 1999)
  • History of food allergy or hypersensitivity to any component of EVOO
  • Participation in a clinical trial carried out with drugs or use of a drug in experimental state during the year prior to inclusion
  • Institutionalized patients for chronic treatment, with lack of autonomy and with inability to perform the clinical follow-up,
  • Impossibility of telephone contact
  • Patients with acute infection or inflammatory process (e.g. pneumonia) may be included in the study three months after the resolution of the infectious symptoms.

结局指标

主要结局

atrial tachyarrhythmias documented by electrocardiogram or recorder device

时间窗: mean follow up of 2 years

Atrial tachyarrhythmia is defined at any fast rate (\>100 bpm) of supraventricular origin lasting more than 30 seconds and that is documented by ECG, Holter or event monitor.

次要结局

  • Atrial fibrillation documented by electrocardiogram or recorder device(mean follow up of 2 years)
  • Changes in quality of life measured by SF-36 questionnaire(mean follow up of 2 years)
  • changes in Inflammatory markers in blood samples(1 year follow up)

研究者

发起方
Fundación de investigación HM
申办方类型
Other
责任方
Principal Investigator
主要研究者

Teresa Barrio

MD, PhD

Fundación de investigación HM

研究点 (4)

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