HIGHLIGHTS
- who: Stéphanie Genay from the This open, prospective, single-centre randomised study was performed in a perioperative HDU at the Lille University Hospital between September , and December The perioperative HDU has , beds and admits all surgical patients requiring organ support after vascular, endocrine and digestive surgery with an average annual admission rate of , patients. The protocol was approved by the patients' protection committee (CPP Nord-Ouest IV) and registered with the US clinical trials database (ClinicalTrials.gov ID NCT02812927) and with the French medicine agency (ID-RCB number, ANSM). Signed informed consent was obtained from patients . . .
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