跳至主要内容
临床试验/JPRN-UMIN000022422
JPRN-UMIN000022422已完成未知

The efficacy of tolvaptan, a vasopressin V2 receptor antagonist, in patients with congestive heart failure and kidney diseases - The efficacy of tolvaptan in patients with congestive heart failure and kidney diseases

Toyama University Hospital0 个研究点目标入组 30 人开始时间: 2016年6月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
30

研究概览

简要总结

As compared to baseline, urine volume increased at day 7 in 17 responders, whereas urine volume decreased at day 7 in 13 non-responders. Baseline urine cyclic AMP/plasma AVP ratio distributed between 0.25 and 4.01 with median 1.90. The urine cyclic AMP/plasma AVP ratio was a significant predictor of response to tolvaptan, which was adjusted for 6 potential confounders with a cutoff of 1.24.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients under 20 years of age at time of enrolling 2. Serum Na >=145 mEq/L 3. Patients with difficulty in water intake 4. Anuria 5. Patients with severe liver failure or severe congestive heart failure 6. Others deemed ineligible for this trial by physicians

研究者

相似试验