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临床试验/EUCTR2015-001888-39-IT
EUCTR2015-001888-39-IT进行中(未招募)1 期

PHARMACOGENOMICS HYPERTENSION :A NEW APPROACH FOR PERSONALIZED MEDICINE ( PGX - HT ) - PGX-HT

OSPEDALE SAN RAFFAELE0 个研究点开始时间: 2016年9月30日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Patients aged between 25 and 60 years with newly diagnosed mild to moderate essential hypertension ( systolic blood pressure between 140 and 160 mmHg and diastolic blood pressure between 90 and 110 mmHg measured as the average of three consecutive measurements )
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 300
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Known causes of secondary hypertension ;
  • - Pregnant women , nursing mothers or women of childbearing age taking anti - contraceptives ;
  • - Severe hypertension or malignant ;
  • - History of kidney disease ;
  • - Significant renal disease ( creatinine clearance less than 60 ml / min ) ; anuria .
  • - Hypokalemia or hyponatremia refractory ;
  • - Hypercalcemia ;
  • -iperuricemia symptomatic ;
  • - Liver disease ;
  • - Heart disease ( myocardial infarction , atrial fibrillation , etc. ) ;
  • - Diabetes ( fasting glucose > 125 mg / dL ) ;
  • - Treatment with statins ;
  • - Obesity ( BMI > 30 kg / m2 ) ;
  • -HYPERSENSITIVITY known to the study drugs ( ACE inhibitors , hydrochlorothiazide , sulphonamide derivatives ) or any of the excipients .
  • -patients not capable of giving valid consent

研究者

发起方
OSPEDALE SAN RAFFAELE

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