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临床试验/NCT06414759
NCT06414759招募中4 期

Efficacy and Safety of Combination Diuretic Therapy in Patients With Acute Decompensated Heart Failure and Volume Overload

Cairo University1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2024年7月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
110
试验地点
1
主要终点
Urine Output

研究概览

简要总结

This study aims to compare two medications, acetazolamide and metolazone, along with loop diuretics, to see which one works better and is safer for patients with ADHF who have volume overload. By comparing these medications, we hope to learn which one can help these patients the most. This will help doctors choose the best treatment for patients with ADHF and volume overload.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients with ages ≥ 18 years old, and less than 65 years old.
  • For both elective and emergency hospital admissions, patients with a clinical diagnosis of ADHF must exhibit at least one clinical sign indicative of volume overload. These signs may include edema (score 2 or higher), ascites confirmed through echography, or pleural effusion confirmed by chest X-ray or echography or rales on auscultation, or jugular venous pressure greater than10 mm Hg.

排除标准

  • Patient diagnosed with acute kidney injury upon hospital admission based on the presence of any of the following criteria: an increase in SCr by at least 0.3 mg/dL within 48 hours, an increase in SCr to at least 2 times the baseline value, known or presumed to have occurred within the prior 7 days, and a urine volume less than 0.5 ml/kg/hour for a duration of 6 hours.
  • Patients with acute pulmonary edema caused by increased afterload and fluid redistribution to the lungs in the absence or with minimal fluid accumulation.
  • Anticipated exposure to nephrotoxic agents (such as contrast dye) during hospitalization.
  • Patients who exhibit anuria or are undergoing renal replacement therapy or ultrafiltration.
  • Patients with eGFR less than 30 mL/min/1.73m² at the time of screening.
  • Expected use of intravenous inotropes, vasopressors, or nitroprusside during the study.
  • Prior cardiac transplantation and/or utilization of a ventricular assist device.
  • Blood pressure below 90 mmHg or mean arterial pressure below 65 mmHg at the time of recruitment.
  • Patients who are pregnant or breastfeeding.
  • Administration of acetazolamide or metolazone within the one-month period preceding randomization.
  • The usage of any diuretic agent during the treatment phase is not specified in the study protocol, except for mineralocorticoid receptor antagonists.

研究组 & 干预措施

Group 1

Experimental

First group (IV loop Diuretics + oral acetazolamide): patients will receive IV loop diuretic 2 times the outpatient oral (PO) daily dose, and oral loop diuretics will be stopped. In cases where the patient was not previously on oral diuretics, a starting dose of 40 mg of IV furosemide, IV bumetanide 1 mg or a bolus of 20 mg of IV torsemide can be utilized, together with acetazolamide: 500 mg PO once daily.

干预措施: Acetazolamide (Drug)

Group 1

Experimental

First group (IV loop Diuretics + oral acetazolamide): patients will receive IV loop diuretic 2 times the outpatient oral (PO) daily dose, and oral loop diuretics will be stopped. In cases where the patient was not previously on oral diuretics, a starting dose of 40 mg of IV furosemide, IV bumetanide 1 mg or a bolus of 20 mg of IV torsemide can be utilized, together with acetazolamide: 500 mg PO once daily.

干预措施: IV Loop Diuretics (Drug)

Group 2

Experimental

Second group (IV loop diuretics + oral metolazone): patients will receive IV loop diuretic approximately 2 times the outpatient oral daily dose, and oral loop diuretics will be stopped. In cases where the patient was not previously on oral diuretics, a starting dose of 40 mg of IV furosemide, IV bumetanide 1 mg or a bolus of 20 mg of IV torsemide can be utilized, together with metolazone: 5 mg PO once daily.

干预措施: Metolazone (Drug)

Group 2

Experimental

Second group (IV loop diuretics + oral metolazone): patients will receive IV loop diuretic approximately 2 times the outpatient oral daily dose, and oral loop diuretics will be stopped. In cases where the patient was not previously on oral diuretics, a starting dose of 40 mg of IV furosemide, IV bumetanide 1 mg or a bolus of 20 mg of IV torsemide can be utilized, together with metolazone: 5 mg PO once daily.

干预措施: IV Loop Diuretics (Drug)

结局指标

主要结局

Urine Output

时间窗: 48 Hours

Total Urine output Volume

次要结局

  • Body Weight(48 Hours)
  • Diuretic Response(48 Hours)
  • Congestion Score(48 Hours)
  • Bicarbonate Level(48 Hours)
  • Serum Creatinine(48 Hours)
  • eGFR(48 Hours)
  • NT-proBNP/BNP(On admission and before discharge (After 48 hours))
  • Blood Pressure(48 Hours)
  • Potassium Level(48 Hours)
  • Length of Hospital Stay(Up to 2 weeks)
  • Mortality or HF Events(3 Months)

研究者

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

Mohamed Ahmed Naguib Mohamed Abdelmoaty

Teaching Assistant of Clinical Pharmacy

Misr International University

研究点 (1)

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