Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
RWTH Aachen University
According to international guidelines a coronary angiography has to be performed within 72h for patients with (NSTEMI).
Patients with a GRACE score \> 140 belong to the high risk group and the coronary angiography has to be performed within 24h.
Until today for patients with a GRACE score \> 140 and an acute or chronic kidney disease (CKD) the best approach is not known even though up to 40% of all NESTMI patients belong to this population. CKD in connection with an NSTEMI is one predictor for short and long term mortality and serious bleeding as a complication of coronary angiography. Additionally patient with CKD are at risk to experience a contrast agent induced aggravation of the CKD right up to a kidney failure. The pre- and post treatment of the kidneys seem to reduce this risk. The irrigation of the kidneys up to 48h prior coronary angiography optimises the kidney function and buffers the aggravation of kidney function caused by fluid loss or abstention at home.
Additionally the influence of ischemic precondition on one arm of the patient will be evaluated in this setting. First studies give a hint that the kidneys may be protected against the contrast agent of the following catheter examination by ischemic precondition.
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
patient with an acute NSTEMI
patient with a GRACE score \< 140
patient with an acute or a chronic kidney disease (stage 1 - 5)
patient who agree with the randomized assignment to one of the study groups in written
signed Informed content prior to study inclusion
patient who are legally competent at the time of study inclusion
You may not be if
pregnancy
nursing women
patient has been committed to an institution by legal or regulatory order
Mental condition rendering the subject unable to understand the nature, scope and possible consequences of the study
participation in a parallel clinical trial
subjects who are in any state of dependency to the investigators