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临床试验/NCT03343340
NCT03343340Unknown不适用

Early Versus Late CRRT (Continuous Renal Replacement Therpay) in ACLF (Acute on Chronic Liver Failure) Patients With Septic Shock and AKI (Acute Kidney Injury) - A Randomized Controlled Trial

Institute of Liver and Biliary Sciences, India1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2017年9月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
150
试验地点
1
主要终点
Transplant Free Survival

研究概览

简要总结

Consecutive patients with ACLF (Acute on Chronic Liver Failure) and septic shock with AKI (Acute Kidney Injury) who give written informed consent will be included in this prospective trial at ILBS. At baseline s, endotoxin levels, NT-Pro BNP, , urine N-GAL will be done for all patients. A 10 ml serum sample will be stored for doing a cytokine profile. Septic shock will be defined by the presence of two or more diagnostic criteria for the systemic inflammatory response syndrome, proven or suspected infection with hypotension non-responsive to adequate fluid resuscitation assessed by no evidence of stroke volume variation on flow track and need of a vasopressor to achieve a target mean arterial pressure (MAP) of ≥ 65 mm Hg. A record of CVP, IVC diameter and B-lines on ultrasound lung would also be done. Patients with age less than 18 years, severe known cardiopulmonary disease (structural or valvular heart disease, coronary artery disease, COPD) pregnancy, chronic kidney disease, patients already meeting emergency criteria for immediate hemodialysis at the time of randomization as specified in the late group, patients transferred from other hospitals who have already been on hemodialysis before their arrival in the intensive care unit, extremely moribund patients with an expected life expectancy of less than 24 hours, failure to give informed consent from family members.

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
None

入排标准

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

入选标准

  • •Patients with ACLF defined based on APASL criteria with septic shock associated AKI

排除标准

  • •Patients with age less than 18 years
  • •Severe known cardiopulmonary disease (structural or valvular heart disease, coronary artery disease, COPD)
  • •Pregnancy
  • •Chronic kidney disease on hemodialysis
  • •Patients with Hepatorenal Syndrome, post renal obstructive AKI, AKI due to glomerulonephritis, interstitial nephritis or vasculitis
  • •Patients already meeting emergency criteria for immediate hemodialysis at the time of randomization as specified in the late group (serum potassium>6 meq/lt, metabolic acidosis ph<7.12, acute pulmonary edema, severe volume overload with hypoxemia non-responsive to diuretic treatment)
  • •Patients transferred from other hospitals who have already been on hemodialysis before their arrival in the intensive care unit
  • •Extremely moribund patients with an expected life expectancy of less than 24 hours
  • •Failure to give informed consent from family members.
  • •Hemodynamic instability requiring very high dose of vasopressors

研究组 & 干预措施

Early CRRT

Experimental

Early Continous Renal Replacement Therapy within 6 hours + Standard Medical Therapy

干预措施: Early CRRT (Other)

Early CRRT

Experimental

Early Continous Renal Replacement Therapy within 6 hours + Standard Medical Therapy

干预措施: Standard Medical Therapy (Other)

Late CRRT

Active Comparator

Late Continous Renal Replacement Therapy + Standard Medical Therapy

干预措施: Late CRRT (Other)

Late CRRT

Active Comparator

Late Continous Renal Replacement Therapy + Standard Medical Therapy

干预措施: Standard Medical Therapy (Other)

结局指标

主要结局

Transplant Free Survival

时间窗: 28 days

次要结局

  • Improvement in lactic acidosis and lactate clearance at 24 hours after initiation of CRRT(within 24 hours)
  • Recovery in renal functions defined as an increase in urine output to more than 400 ml/day(1 year)
  • Duration of mechanical ventilation and ICU (Intensive Care Unit) stay(1 year)
  • Improvement in SOFA (Sequential Organ Failure Assessment ) ( by 2 points) scores(1 year)
  • Achievement of target ultrafiltration goals(1 year)
  • Incidence of intradialytic hypotension i.e. defined as a decrease in systolic blood pressure by ≥20 mm Hg or a decrease in MAP by 10 mm Hg associated with symptoms(1 year)
  • Hemodynamic stability i.e. maintenance of MAP on dialysis without increase in the vasopressors(1 year)
  • Dialysis efficiency as measured by Urea Reduction ratio at 48 hours(2 days)
  • Improvement in APACHE (Acute Physiology and Chronic Health Evaluation) ( by 2 points) scores(1 year)
  • Improvement in MELD (Model for End Stage Liver Disease) ( by 2 points) scores(1 year)
  • Improvement in lactic acidosis and lactate clearance at 6 hours after initiation of CRRT(within 6 hours)
  • Improvement in lactic acidosis and lactate clearance at 12 hours after initiation of CRRT(within 12 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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