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临床试验/NCT00736866
NCT00736866已完成3 期

A Pragmatic Randomized Clinical Trial Evaluating the Effect of Acetylcysteine for Contrast-induced Nephropathy

Hospital do Coracao1 个研究点 分布在 1 个国家目标入组 2,300 人开始时间: 2008年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
2,300
试验地点
1
主要终点
Contrast-induced nephropathy incidence

研究概览

简要总结

The purpose of this study is to evaluate the efficacy of acetylcysteine compared to placebo for the contrast-induced nephropathy prevention, between 48 and 96 hours after procedures that use contrast.

Contrast-induced nephropathy is defined as an increase of 25% in serum creatinine before the procedure.

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

  • At least one of the following criteria:
  • Aged more than 70 years-old
  • Chronic renal failure (defined as serum creatinine higher than 1.5mg/dL within the last 3 months)
  • Diabetes mellitus
  • Congestive heart failure or ventricular disfunction (left ventricular ejection fraction less than 0.45)
  • Shock or intra-aortic balloon pump use
  • Urgency or emergency procedures

排除标准

  • Pregnant women, breastfeeding or aged below 45 years-old and with no efficacious contraceptive methods.
  • Patients in dialysis
  • Previous inclusion in this trial
  • Patient refusal to informed consent
  • Pacientes com Infarto Agudo do Miocárdio com supradesnivelamento do segmento S-T nos quais não seja possível administrar o protocolo de hidratação pré e pós-procedimento.

研究组 & 干预措施

Acetylcysteine

Experimental

干预措施: Acetylcysteine (Drug)

Control

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Contrast-induced nephropathy incidence

时间窗: between 48 and 96 hours after angiographic procedures

次要结局

  • Combined outcome of total mortality, dialysis indication or basal serum creatinine duplication(within 30 days)
  • Combined outcome of total mortality or dialysis indication(within 30 days)
  • The individual components of the combined outcome(within 30 dias)

研究者

申办方类型
Other

研究点 (1)

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