跳至主要内容
临床试验/NCT00334581
NCT00334581已完成4 期

A Study of Irbesartan 150mg Verses 300mg in Chinese Hypertensive Patients With Diabetes and Microalbuminuria

Sanofi1 个研究点 分布在 1 个国家目标入组 192 人开始时间: 2006年5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
发起方
Sanofi
入组人数
192
试验地点
1
主要终点
The difference of urinary albumin excretion rate change

研究概览

简要总结

Primary objective:

  • To determine if irbesartan 300mg is better than 150mg in protecting the kidneys in hypertensive patients with diabetes and microalbuminuria.

Secondary objectives:

  • To determine how well irbesartan 300mg is tolerated versus 150mg
  • To determine the percentage of patients reaching the blood pressure target of 130/80 mmHg

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
None

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Hypertensive patients, treated or untreated, with type 2 diabetes and urinary albumin excretion rate 20-200ug/min.
  • Blood pressure of < 180/110mmHg at baseline
  • Normal serum creatinine

排除标准

  • Type 1 diabetes
  • Use of angiotensin converting enzyme inhibitors or angiotensin receptor blockers in the 5 weeks before recruitment
  • Pregnant or lactating women
  • Severe hypertension
  • Overt nephropathy
  • Allergy to study drug
  • The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

研究组 & 干预措施

1

Experimental

Irbesartan 150mg

干预措施: Irbesartan (Drug)

2

Experimental

Irbesartan 300mg

干预措施: Irbesartan (Drug)

结局指标

主要结局

The difference of urinary albumin excretion rate change

时间窗: at week 24

次要结局

  • Percentage of patients reaching target BP of 130/80mmHg(At week 24)
  • Adverse events(From the beginning to the end of the study)

研究者

发起方
Sanofi
申办方类型
Industry

研究点 (1)

Loading locations...

相似试验