https://www.selleckchem.com/products/art0380.html
The trial will enrol 274 participants across multiple London National Health Service ICUs. The trial will use a primary outcome of duration of mechanical ventilation until successful extubation. Safety oversight will be under the direction of an independent committee of the study sponsor. Study approval was obtained from the regional ethics committee of the Health Research Authority (HRA), (Research Ethic Committee (REC) reference 17/LO/0887. Integrated Research Application System (IRAS) reference 226610. Results will be disseminated th
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