Seattle Cardiorenal Remote Ischemic Preconditioning Trial
Completed · Not applicable
Conditions studied: Congenital Heart Disease, Cardiopulmonary Bypass, Myocardial Injury, Acute Kidney Injury, Acute Lung Injury
In brief
Remote Ischemic Preconditioning (RIPC) is a treatment that may be associated with improved outcomes after cardiac surgery. It can be elicited noninvasively by using a tourniquet to elicit transient ischemia over a lower extremity. It is thought to promote anti-inflammatory and cell survival pathways, and thus protect remote organs against future ischemic injury. We hypothesize that compared to sham treatment, RIPC will be associated with decreased post-operative acute kidney, myocardial, and lung injury.
Key facts
- Study ID
- NCT01260259
- Run by
- Seattle Children's Hospital
- People needed
- 90
- Starts
- 2010-12-01
- Expected to finish
- 2013-08-01
- Last updated by the study team
- 2013-09-18
Who can join
Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age birth to 18 years Cardiac surgery with planned cardiopulmonary bypass
You may not qualify if…
- Any contraindication to compression of lower extremity/extremities Body weight <2 kg Active infection going into surgery On renal replacement therapy (RRT) or mechanical circulatory support going into surgery On inotropic support going into surgery
Where it is running
- Seattle Children's Hospital — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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