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临床试验/NL-OMON34436
NL-OMON34436尚未招募3 期

Perindopril arginine/Amlodipine versus Valsartan/Amlodipine antihypertensive startegies: Efficacy and safety in mild to moderate hypertensive patients. A randomised, double blind 6-month study followed by 8-month open label long-term follow-up with Perindopril arginine/Amlodipine. - Efficacy/safety of Perindoprilarg./Amlodipine versus Valsartan/Amlodipine

Servier R&D Benelux0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Patients women and men of at least 18 years with BMI*30:
  • For untreated patients: 150*SBP<180 mmHg and 95mmHg*DBP <110mmHg
  • For treated patients with no more than2 antihypertensive drugs and who in the investigator*s opinion require a change in medication either because of insufficient efficacy or poor tolerability: SBP <160 mmHg and DBP<100 mmHg.;Inclusion visit
  • After two weeks placebo run-in period 150*SBP<180 mmHg and 95mmHg*DBP <110mmHg
  • Tablet compliance *70%and* 130%during placebo period

排除标准

  • Patients treated with more than 2 antihypertensive drugs at the selection visit or treated with Perindopril arginine/Amlodipine or Valsartan/Amlodipine free or fixed combination at the highest available doses (P10/A 10 mg or V160/A10 mg).
  • History of intolerance with one or several study drugs
  • Contraindication for using the study drugs
  • History of acute episode of cerebrovascular disease, acute episode of heart disease
  • alcholism or drug abuse
  • Secondary hypertension , known symptomatic orthostatic hypotension
  • Pregnancy, breastfeeding or possibilty to become pregnant during the study;Inclusionvisit
  • Presence on the selection ECG of ventricular rhytm disorders: twisting spikes, ventricular tachycardia, ventricular extra-systoles (except for isolated occurence) or atrial fibrillation or atrial flutter or other cardiac rhytm disorders leading to important beat-to-beat variations in blood pressure
  • Positive orthostatic test at inclusion
  • Selection Laboratory result unavailable
  • Hyponatraemia (<135 mmol/L) or hypernatraemia (>150 mmol/L), hypokalaemia (<3.5 mmol/L) or hyperkalaemia (>5.8 mmol/L).
  • Creatinine clearance <30ml/min,using Cockcroft*s formula
  • ALAT or ASAT upper than 3 times the upper limit of normal laboratory range
  • Positive pregnancy test (beta GCH) performed at selection visit

研究者

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