跳至主要内容
临床试验/EUCTR2006-005408-14-CZ
EUCTR2006-005408-14-CZ进行中(未招募)不适用

A 14 week extension to a randomized, double-blind, multicenter, parallel-group, active-controlled study to evaluate the long term safety, tolerability and efficacy of valsartan and enalapril combined and alone in children 6 to 17 years of age with hypertension

ovartis Pharma Services AG0 个研究点目标入组 270 人开始时间: 2007年5月22日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
270

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

  • Please refer to CVAL489K2302 for complete details related to the inclusion and exclusion criteria for the core study.
  • Additional inclusion criteria:
  • - Successful completion of 12 weeks of double blind treatment in core protocol
  • CVAL489K2302
  • - Discontinueing prematurely from teh core CVAL489K2302 study due to
  • uncontrolled hypertension defined as; MSSBP>20%, but ><25% above the 95th
  • percentile for age, gender, and height after visit 5, qualifies a patient for entry into
  • this extension study.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Please refer to CVAL489K2302 for complete details related to the inclusion and exclusion criteria for the core study.
  • Additional exclusion criteria:-
  • - Patients who experienced any adverse events considered serious and drug
  • related in protocol CVAL489K2302 are exluded.

研究者

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