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临床试验/NCT02665377
NCT02665377已完成3 期

Prevention of Akute Kidney Injury With Human Atrial Natriuretic Peptide in Patients Undergoing Heart Transplant.

Sahlgrenska University Hospital, Sweden1 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2016年9月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
86
试验地点
1
主要终点
GFR 4-5 days after Htx

研究概览

简要总结

Prospective, blinded, placebo-controlled trial. Patients: Adult patients (>18 years of age) undergoing de novo Htx, with a preoperative GFR > 30ml/min, not receiving an ABO-incompatible organ with an ischemia time of > 6 hours. A donor age > 70 years is an exclusion criteria.

Intervention: Infusion of h-ANP fore five days, starting at the induction of anesthesia.

Outcome: Kidney function, evaluated with serum creatinine day 1-7 and kidney clearance, 4-5 Days after Htx plus after 3 and 12 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
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

  • De novo Htx.
  • Preoperative GFR > 30ml/min/1,73m
  • >18 years old.
  • Written consent.

排除标准

  • Multi organ transplantation or previous heart transplant.
  • Donor age > 70 years.
  • Dialysis.
  • ABO-incompatible organ.
  • Donor heart ischemia time > 6 tim.
  • Known kidney disease.
  • Other planed study within 2 mounth.

研究组 & 干预措施

ANP

Active Comparator

Infusion of h-ANP at dose of 50ng/kg/min fore 5 days, starting at the induction of anesthesia.

干预措施: ANP (Drug)

Placebo

Placebo Comparator

Infusion of NaCl at the same volyme as for ANP for 5 days.

干预措施: Placebo (Drug)

结局指标

主要结局

GFR 4-5 days after Htx

时间窗: 4-5 days

次要结局

  • GFR 1 year after Htx(1 year)

研究者

发起方
Sahlgrenska University Hospital, Sweden
申办方类型
Other
责任方
Principal Investigator
主要研究者

Maria Tholén

MD

Sahlgrenska University Hospital, Sweden

研究点 (1)

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