跳至主要内容
临床试验/NCT02315976
NCT02315976已完成4 期

Avaliação de episódios Agudos na Angina Pectoris crônica estável: Abordagem clínico-laboratorial do Uso do Vasodilatador Coronariano Propatilnitrato.

Fundação Educacional Serra dos Órgãos1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2014年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
200
试验地点
1
主要终点
Number of angina episodes

研究概览

简要总结

This is an open, self-paired study of 200 patients with heart failure who have a diagnosis of chronic stable angina pectoris, who will be treated for 30 days with propatyl nitrate (10mg) . Treatment regimen is 3 sublingual tablets per day, at 8:00 AM, 2:00 PM, and 8:00 PM. The study will include three visits the patient to the study center: Pretreatment / Assessment 1, Assessment 2 after 15 days of treatment, and the Assessment 3 after 30 days of treatment. At each visit, data will be collected on the medical history, physical examination and vital signs, and evaluation of episodes of angina pectoris, as well as the laboratory evaluation of adverse events and the use of concomitant medications.

研究设计

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

入排标准

年龄范围
50 Years 至 68 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of chronic stable angina pectoris
  • Female subjects post-menopausal or not pregnant and using of contraceptives
  • Signature of Informed consent document

排除标准

  • Pregnant women or nursing patients , women of childbearing age
  • Hypersensitivity or intolerance to any component of the study drug
  • Angina pectoris Class IV, according to the Canadian Society of Cardiology
  • Clinical diagnosis of severe anemia , glaucoma, head trauma , increased intracranial pressure, cerebral hemorrhage, acute myocardial infarction, congestive heart failure, aortic valve disease
  • Recent infarction (within the last 3 months)
  • Recent history (within the last 6 months)of angioplasty
  • Use of these medicines within 7 days screening : sildenafil citrate and other inhibitors of phosphodiesterase-5 , adrenergic substances
  • Significant alteration of any laboratory test (> 20% above or below the normal range )
  • Gastric or intestinal ulcer or intestinal
  • Asthma or chronic rhinitis
  • Any other condition which in the opinion of the investigator, shall exclude the study of the patient.

研究组 & 干预措施

Propatyl nitrate

Experimental

Patients treated with propatyl nitrate 10mg thrice daily

干预措施: Propatyl Nitrate (Drug)

结局指标

主要结局

Number of angina episodes

时间窗: 30-day treatment period

Number of angina episodes per patient during the 30 day treatment period

次要结局

  • Adverse Event - occurence(30-day treatment period)
  • Episode duration(30-day treatment period)
  • Pain intensity(30-day treatment period)
  • Seattle Angina Questionnaire (SAQ) scales score improvements(30-day treatment period)
  • Seattle Angina Questionnaire (SAQ) Score increase >30%(30-day treatment period)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Carlos Pereira Nunes

Professor of Internal Medicine

Fundação Educacional Serra dos Órgãos

研究点 (1)

Loading locations...

相似试验