跳至主要内容
临床试验/NCT02427880
NCT02427880已完成4 期

Acetazolamide and Hydrochlorothiazide Followed by Furosemide Versus Hydrochlorothiazide and Furosemide Followed by Furosemide for the Treatment of Adults With Refractory Nephrotic Edema: A Randomized, Double-Blind Trial

Shiraz University of Medical Sciences0 个研究点目标入组 20 人开始时间: 2015年4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
入组人数
20
主要终点
Change from baseline in weight at the end of third week

研究概览

简要总结

The purpose of this study is to determine whether using furosemide following acetazolamide is effective in treating refractory edema associated with nephrotic syndrome.

详细描述

Edema is referred to increase in interstitial fluid that is clinically evident. The main causes of generalized edema are heart failure, renal failure, nephrotic syndrome, glomerulonephritis and chronic liver failure. In some cases, edema is treated by management of the underlying disease. However, in some other cases edema may persist and become more severe that needs adjuvant treatments. Because use of diuretics such as furosemide and hydrochlorothiazide is not completely effective in treating severe refractory edema, use of some other diuretics is also recommended. In this double-blind clinical trial, weight and some lab data including blood urea nitrogen, serum creatinine, serum sodium, serum potassium, serum albumin, urine sodium, urine potassium, 24-hour urine volume, 24-hour urine protein and 24-hour urine creatinine of 20 random adult patients with nephrotic syndrome who have refractory edema and GFR>60 ml/min/1.73m2 and are referred to nephrology clinic of Shiraz University of Medical Sciences will be measured; the patients should not have hypokalemia and other causes of edema such as heart failure or cirrhosis. Then the patients are divided into 2 groups with 10 members in each. The first group will be prescribed 40 mg of furosemide and 50 mg of hydrochlorothiazide and the second one will receive 250 mg of acetazolamide and 50 mg of hydrochlorothiazide daily for 1 week. Then, weight and mentioned lab data will be measured again. After that, all the patients will have 40 mg of furosemide daily for 2 weeks. Then, weight and mentioned lab data will be measured for one more time.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Having refractory edema due to nephrotic syndrome
  • Having GFR>60 ml/min/1.73m2
  • Being able to come for weekly visit
  • Having the minimum age of 18 years
  • Signing the informed consent form

排除标准

  • Hypokalemia
  • Renal transplant
  • active malignancy or infection
  • Using NSAIDs
  • Having another causes of edema including liver cirrhosis, heart failure
  • Neurologic or psychiatric problem hindering adherence to the study protocol

研究组 & 干预措施

Acetazolamide

Experimental

Each patient receives 250 mg of acetazolamide and 50 mg of hydrochlorothiazide daily for 1 week. Then they are prescribed 40 mg of furosemide daily for 2 weeks.

干预措施: Acetazolamide and Hydrochlorothiazide Followed by Furosemide (Drug)

Furosemide

Active Comparator

Each patient is prescribed 40 mg of furosemide and 50 mg of hydrochlorothiazide daily for 1 week. Then they receive 40 mg of furosemide daily for 2 weeks.

干预措施: Furosemide and Hydrochlorothiazide Followed by Furosemide (Drug)

结局指标

主要结局

Change from baseline in weight at the end of third week

时间窗: Baseline and at the end of the third week

次要结局

  • Change from baseline in 24-hour urine volume at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in 24-hour urine creatinine at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in serum sodium at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in serum albumin at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in urine sodium at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in systolic and diastolic blood pressure at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in serum potassium at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in blood urea nitrogen at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in serum creatinine at the end of third week(At the start and at the end of the third week)
  • Change from baseline in 24-hour urine protein at the end of third week(Baseline and at the end of the third week)
  • Change from baseline in urine potassium at the end of third week(Baseline and at the end of the third week)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammad Amin Fallahzadeh

MD-MPH

Shiraz University of Medical Sciences

相似试验