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临床试验/NCT01349348
NCT01349348已完成3 期

A Randomized, Double-blinded, Multicenter, Placebo Controlled, Parallel Designed Study, to Evaluate the Efficacy and Safety of Tolvaptan Tablet in Treatment of Patients With Cirrhosis Ascites, Using Diuretics as Initial Treatment

Otsuka Beijing Research Institute1 个研究点 分布在 1 个国家目标入组 535 人开始时间: 2010年10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
入组人数
535
试验地点
1
主要终点
Change from baseline in body weight after 7 days randomized treatment (Day 8).

研究概览

简要总结

To evaluate the efficacy and safety of Tolvaptan 7.5mg and 15mg in treatment of patients with cirrhosis ascites who fail to response adequately to treatment with common diuretics.

详细描述

For symptoms of fluid retention due to liver diseases (ascites and/or lower extremity edema, i.e. hepatic edema), treatment generally starts with bed rest and a low-salt diet. Aldosterone antagonists and loop diuretics are commonly used diuretics in the treatment of fluid retention due to liver diseases. In aldosterone antagonists' therapy, nevertheless, hyperkalemia is frequently reported, slow onset of action and dose escalation needed also impair its effect. If aldosterone antagonists' therapy is ineffective, loop diuretics as strong diuretics are usually added up. However, Dose escalation of loop diuretics also boost the occurrence of hyponatremia and hypokalemia, and combination of the two drugs provided fastest onset of effectiveness with less adverse events. While, because both diuretics can cause sodium lose which is difficult to prevent and treat, hyponatremia is easy to occur. The combination of aldosterone antagonists and K-sparing diuretics reduces the occurrence of hypokalemia but have little effect on the prevention and treatment of hyponatremia. In addition, there are still some patients who are resistent to loop diuretics or intolerant of an effective diuretic dosage due to adverse events.

Tolvaptan increases the excretion of electrolyte-free water (aquaretic) without changing electrolytes excretion by inhibiting the water reabsorption of collecting duct in kidney. It is demonstrated that Tolvaptan increased urine volume without impairing renal function.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Tolvaptan 15mg

Experimental

Tablet;15mg/tab

干预措施: Tolvaptan (Drug)

Tolvaptan 7.5mg

Experimental

Tablet;7.5mg/tab

干预措施: Tolvaptan (Drug)

Placebo

Placebo Comparator

Tolvaptan 0mg/tab

干预措施: placebo (Drug)

结局指标

主要结局

Change from baseline in body weight after 7 days randomized treatment (Day 8).

时间窗: 7 days

次要结局

  • Change from baseline in body weight after 4 days randomized treatment (Day 5);(4days)
  • The rate of change from baseline in body weight after 4, 7 days randomized treatment (Day 5, Day 8);(4 and 7 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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