跳至主要内容
临床试验/NCT00147563
NCT00147563已完成4 期

A Double-Blind, Parallel Design Study to Compare the Effectiveness of Eplerenone Versus Atenolol in Reversing the Remodeling of Resistance Arteries in Subjects With Mild to Moderate Primary Hypertension

Pfizer2 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2003年10月最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
Pfizer
入组人数
34
试验地点
2
主要终点
The change from baseline to week 52 in the media/lumen ratio and the maximum % relaxation response to acetylcholine of gluteal subcutaneous resistance vessels, measured from the gluteal biopsy.

研究概览

简要总结

To investigate the impact of antihypertensive therapy with the selective mineralocorticoid receptor blocker, eplerenone, on small resistance artery remodeling, compared to the effect of equivalent blood pressure control achieved with a b-blocker, atenolol.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pt with essential hypertension who have never been treated or untreated within the previous 6 months

排除标准

  • History of Malignant Hypertension
  • Sitting diastolic blood pressure > 115mmHg or sitting Systolic blood pressure > 200mmHg

结局指标

主要结局

The change from baseline to week 52 in the media/lumen ratio and the maximum % relaxation response to acetylcholine of gluteal subcutaneous resistance vessels, measured from the gluteal biopsy.

次要结局

  • Will be done for both the Intent to Treat and per protocol populations, and use both the LOCF and OC methods

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (2)

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