Preconditioning Against Renal Damage Under Contrast Examination (Re-DUCE-F)
Acute Kidney Injury
About this trial
This is an interventional prevention trial for Acute Kidney Injury focused on measuring Computerized Tomography, Contrast enhanced, Acute Kidney Injury, Remote ischaemic preconditioning, RIPC
Eligibility Criteria
Inclusion Criteria:
- All medical and surgical in-patients aged 40-yrs or over scheduled to undergo contrast-enhanced CT scans.
- Patients willing to give full informed consent for participation
Exclusion Criteria:
- Pregnancy
- Significant upper limb peripheral arterial disease
- Previous history of upper limb deep vein thrombosis
- Patients on glibenclamide or nicorandil (these medications may interfere with RIPC)
- Patients with an estimated pre-operative glomerular filtration rate <30mls/min/1.73m2
- Patients with a known history of myocarditis, pericarditis or amyloidosis
- Patients who have received intravenous contrast in the previous year
- Patients with severe hepatic disease defined as a an international normalised ratio >2 in the absence of systemic anticoagulation
- Patients previously enrolled in the trial representing a further scan
Sites / Locations
- University Hospital LimerickRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
RIPC
Control
Preconditioning will be performed in the same manner as several previous trials. Immediately prior to having the CT scan a CE-approved blood pressure cuff will be placed around one arm of the patient. It will then be inflated to a pressure of 200mmHg for 5 minutes. For patients with a systolic blood pressure >185mmHg, the cuff will be inflated to at least 15mmHg above the patient's systolic blood pressure. The cuff will then be deflated and the arm allowed reperfuse for 5 minutes. This will be repeated so that each patient receives a total of 4 ischaemia-reperfusion cycles.
Patients randomised to this group will receive routine care associated with undergoing a CT scan.