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临床试验/NCT02173288
NCT02173288已完成2 期

Role of Midodrine and Tolvaptan in Patients With Cirrhosis With Refractory or Recurrent Ascites

Post Graduate Institute of Medical Education and Research, Chandigarh1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
50
试验地点
1
主要终点
Number of patients with control of ascites

研究概览

简要总结

The development of ascites in the natural history of cirrhosis heralds a worsening of the prognosis to 50% survival at 2 years, and this deteriorates to 30-50% at 1 year when the ascites becomes refractory to medical therapy. Hemodynamic alterations and their relation to neurohumoral systems are essential in pathophysiology of ascites formation. The theory that best explain the ascites formation and sodium retention in cirrhotics is portal hypertension leading to splanchnic arterial vasodilatation leading to underfilling of arterial circulation which is sensed by the arterial and the cardiopulmonary receptors leading to sympathetic nervous system activation and activation of the anti-natriuretic factors (RAAS and arginine vasopressin), resulting in sodium and water retention. The therapeutic options available for patients with refractory ascites are serial therapeutic paracentesis, liver transplantation and transjugular intrahepatic portosystemic shunts.Vasopressin V2 receptor antagonists antagonize the antidiuretic effects of vasopressin at the V2 receptor located in the renal collecting duct, they increase free water clearance, and thus may be helpful in mobilizing excess water in conditions associated with water retention including cirrhosis. The use of V2 receptor antagonists in cirrhosis with ascites has been shown to be safe and efficacious. Midodrine, an alpha adreno receptor agonist by causing splanchnic vasoconstriction has been used in hepatorenal syndrome (HRS) and for control of ascites in patients with refractory or recurrent ascites. It is possible that vasoconstrictors and aquaretics (V2 receptor antagonists) by acting at different sites in combination may reverse some of the pathogenic events that results in refractory or recurrent ascites.There are no reports on the use of combination of midodrine and tolvaptan in the patients with cirrhosis with ascites. Therefore, we plan to study the role of midodrine, tolvaptan and their combination on systemic hemodynamics, renal functions and control of ascites in patients with cirrhosis and refractory or recurrent ascites.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 60 consecutive patients with cirrhosis and refractory or recurrent ascites with stable renal function ( creatinine level <1.5mg/dl for at least 7 days ).

排除标准

  • Presence of gastrointestinal bleeding, HRS, hepatic encephalopathy of grade 2 or higher or infection within 1 month preceding the study or during the study, presence of diabetes, intrinsic renal or cardiovascular disease or arterial hypertension on history and physical examination, abnormal urine analysis, chest radiograph or electrocardiogram, presence of hepatocellular carcinoma or portal vein thrombosis or treatment with drugs with known effects on systemic and renal hemodynamics within 7 days of inclusion .

研究组 & 干预措施

Standard medical therapy

Active Comparator

Standard Medical therapy (n-15) with100 to 400mg spironolactone and/or 40 to 160mg furosemide.

干预措施: Standard medical therapy (Drug)

Midodrine group

Active Comparator

Standard medical therapy (n-15) with Midodrine 7.5 mg thrice a day

干预措施: Standard medical therapy (Drug)

Midodrine group

Active Comparator

Standard medical therapy (n-15) with Midodrine 7.5 mg thrice a day

干预措施: Midodrine (Drug)

Tolvaptan group

Active Comparator

Standard medical therapy (n-15) with Tolvaptan 15 mg twice a day

干预措施: Standard medical therapy (Drug)

Tolvaptan group

Active Comparator

Standard medical therapy (n-15) with Tolvaptan 15 mg twice a day

干预措施: Tolvaptan (Drug)

Tolvaptan plus midodrine arm

Experimental

Standard medical therapy (n-15) with Tolvaptan 15 mg twice a day and Midodrine 7.5 mg thrice a day

干预措施: Standard medical therapy (Drug)

Tolvaptan plus midodrine arm

Experimental

Standard medical therapy (n-15) with Tolvaptan 15 mg twice a day and Midodrine 7.5 mg thrice a day

干预措施: Tolvaptan (Drug)

Tolvaptan plus midodrine arm

Experimental

Standard medical therapy (n-15) with Tolvaptan 15 mg twice a day and Midodrine 7.5 mg thrice a day

干预措施: Midodrine (Drug)

结局指标

主要结局

Number of patients with control of ascites

时间窗: 3 months

Control of ascites will be defined as: Complete: defined as the elimination of ascites Partial: presence of ascites not requiring paracentesis Failure: defined as persistence of ascites requiring paracentesis

次要结局

  • Number of patients with worsening of encephalopathy(3 months)
  • Number of patients with impairment of liver function(3 months)
  • Number of patients with variceal bleed(3 months)
  • Number of patients developing hepatorenal syndrome(3 months)
  • Number of patients with hypernatremia(3 months)

研究者

发起方
Post Graduate Institute of Medical Education and Research, Chandigarh
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr.Virendra Singh

Professor of Hepatology

Post Graduate Institute of Medical Education and Research, Chandigarh

研究点 (1)

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