跳至主要内容
临床试验/NCT01928628
NCT01928628已完成3 期

A Randomized, Multicenter, Parallel Design Phase III Clinical Study to Evaluate the Efficacy and Safety of the Combination of Lercanidipine/Valsartan in Hypertensive Patients Who Are Not Adequately Controlled on Lercanidipine 10mg Monotherapy.

LG Life Sciences1 个研究点 分布在 1 个国家目标入组 449 人开始时间: 2012年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
449
试验地点
1
主要终点
Change in mean sitDBP from week 0 to week 40

研究概览

简要总结

This study aims to compare and assess the efficacy and the safety of the combination agent of Lercanidipine and Valsartan and monotherapy of Lercanidipine alone in patients with essential hypertension

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
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged ≥ 20 to ≤75 years old
  • Patient with essential hypertension

排除标准

  • When the BP level measured at screening was sitDBP>120 mmHg or sitSBP >180 mmHg
  • Patient with difference in repeatedly measured blood pressures from the selected arm at screening was sitSBP≥ 20mmHg or sitDBP ≥ 10mmHg

研究组 & 干预措施

Lercanidipine 10mg

Active Comparator

1 Tablet of Zanidip ® 10mg + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipine 10mg (Drug)

Lercanidipine 10mg

Active Comparator

1 Tablet of Zanidip ® 10mg + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipine10mg /Valsartan 80mg Placebo (Drug)

Lercanidipine 10mg

Active Comparator

1 Tablet of Zanidip ® 10mg + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipine 10mg /Valsartan 160mg Placebo (Drug)

Lercanidipine10mg /Valsartan 80mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo +1 Tablet of L10/V80 + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipine10mg /Valsartan 80mg (Drug)

Lercanidipine10mg /Valsartan 80mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo +1 Tablet of L10/V80 + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipin 10mg Placebo (Drug)

Lercanidipine10mg /Valsartan 80mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo +1 Tablet of L10/V80 + 1 Tablet of L10/V160 Placebo (8wks)

干预措施: Lercanidipine 10mg /Valsartan 160mg Placebo (Drug)

Lercanidipine 10mg /Valsartan 160mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/ V160 (8wks)

干预措施: Lercanidipine 10mg /Valsartan 160mg (Drug)

Lercanidipine 10mg /Valsartan 160mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/ V160 (8wks)

干预措施: Lercanidipin 10mg Placebo (Drug)

Lercanidipine 10mg /Valsartan 160mg

Experimental

1 Tablet of Zanidip ® 10mg Placebo + 1 Tablet of L10/V80 Placebo + 1 Tablet of L10/ V160 (8wks)

干预措施: Lercanidipine10mg /Valsartan 80mg Placebo (Drug)

结局指标

主要结局

Change in mean sitDBP from week 0 to week 40

时间窗: 40 weeks

次要结局

  • Response rate at week 4 and 8(4 weeks and 8 weeks)

研究者

发起方
LG Life Sciences
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验