跳至主要内容
临床试验/ISRCTN62869767
ISRCTN62869767已完成未知

Multi-centre randomised controlled trial of angiotensin converting enzyme inhibitor (ACEi)/angiotensin receptor blocker (ARB) withdrawal in advanced renal disease: the STOP-ACEi trial

Hull University Teaching Hospitals NHS Trust0 个研究点目标入组 411 人开始时间: 2014年2月25日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
411

研究概览

简要总结

2016 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/26429974 protocol 2022 Results article in https://pubmed.ncbi.nlm.nih.gov/36326117/ (added 07/12/2022)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged =18 years (male or female)
  • 2. CKD stage 4 or 5 (eGFR <30 ml/minute using the MDRD equation) and not on dialysis therapy
  • 3. Progressive deterioration in renal function (fall in eGFR of >2 ml/min/year over previous 12-24 months) as measured by linear regression analysis. A simple excel spreadsheet for calculation of this will be provided to all sites. A minimum of 3 measurements of eGFR over the previous 12-24 months are required to identify a >2 ml/min/year fall. The last eGFR must be within 3 months of randomisation
  • 4. Treatment with either an ACEi or ARB, or a combination of both, for >6 months with at least 25% of the maximum recommended daily dose on the day of consent
  • 5. Resting blood pressure (BP) =160/90 mmHg when measured in accordance with British Hypertension Society guidelines in clinic or home blood pressure readings within the previous month or a 24 h ambulatory blood pressure measurement within the last 3 months are acceptable
  • 6. At least 3 months of specialist renal follow-up at the time of entry into the trial
  • 7. Written, signed informed consent to the trial

排除标准

  • 1. Aged <18 years
  • 2. Uncontrolled hypertension (>160/90 mmHg) or requirement for 5 or more agents to control BP
  • 3. Undergoing dialysis therapy
  • 4. Any condition which, in the opinion of the investigator, makes the participant unsuitable for trial entry due to prognosis/terminal illness with a projected survival of less than 12 months
  • 5. History of myocardial infarction or stroke in preceding 3 months
  • 6. Participation in an interventional research study in preceding 6 weeks
  • 7. Pregnancy, confirmed by positive pregnancy test, or breastfeeding
  • 8. Inability to provide informed consent (e.g. due to cognitive impairment)
  • 9. Immune-mediated renal disease requiring disease-specific treatment
  • 10. Known drug or alcohol abuse
  • 11. Inability to comply with the trial schedule and follow-up

研究者

相似试验