4.5 Article

Effect of remote ischaemic conditioning on contrast-induced nephropathy in patients undergoing elective coronary angiography (ERICCIN): rationale and study design of a randomised single-centre, double-blind placebo-controlled trial

Journal

CLINICAL RESEARCH IN CARDIOLOGY
Volume 103, Issue 3, Pages 203-209

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00392-013-0637-3

Keywords

Remote ischaemic conditioning; Preconditioning; Contrast-induced nephropathy; Acute kidney injury; Clinical trial; Coronary angiography; Percutaneous intervention

Funding

  1. British Heart Foundation [RG/08/015/26411]
  2. Department of Health's National Institute of Health Research (NIHR) Biomedical Research Centres (BRC)
  3. NIHR BRC Cardiometabolic funding award
  4. MRC [MR/K002066/1] Funding Source: UKRI
  5. British Heart Foundation [RG/08/015/26411] Funding Source: researchfish
  6. Medical Research Council [MR/K002066/1] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0510-10164] Funding Source: researchfish

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Contrast-induced nephropathy (CIN), an acute kidney injury resulting from the administration of intravascular iodinated contrast media, is an important cause of morbidity/mortality following coronary angiographic procedures in high-risk patients. Despite preventative measures intended to mitigate the risk of CIN, there remains a need for an effective intervention. Remote ischaemic conditioning (RIC), where non-injurious ischaemia is applied to an arm prior to the administration of contrast, has shown promise in attenuating CIN but its effectiveness in preserving long-term renal function is unknown, which will be studied as part of the effect of remote ischaemic conditioning against contrast-induced nephropathy (ERICCIN) trial. Identifier: ISRCTN49645414.) The ERICCIN trial is a single-centre, randomised double-blinded placebo-controlled trial which plans to recruit 362 patients who are at risk of CIN, defined by pre-existent renal impairment (estimated glomerular filtration rate < 60 ml/min/1.73 m(2)), over a period of 2 years. Patients will be randomised to either control or RIC consisting of 4, 5 min 200 mmHg balloon-cuff inflation/deflations, to the upper arm. The primary endpoint will be the development of CIN (> 25 % of eGFR, or rise of creatinine of > 44 mu mol/l) at 48 h. A key secondary endpoint will be whether RIC impacts upon persistent renal impairment over the 3-month follow-up period. Additional secondary endpoints include the measurement of serum neutrophil gelatinase-associated lipocalin and urinary albumin at 6, 48 h and 3 months following administration of contrast. Findings from ERICCIN trial will potentially demonstrate that RIC attenuates contrast-induced acute and chronic kidney injury and influence future clinical practice guidelines in at-risk patients undergoing coronary angiographic procedures.

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