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Description
Preliminary safety and efficacy of L-carnitine infusion for the treatment of vasopressor-dependent septic shock: A randomized control trial
80.9 1.8 kg, p = 0.007) after carnitine supplementation for 4 weeks (44), a minimum sample size of 17 was determined for each group, which was increased to 23, anticipating a dropout rate of 35%, using the Power Analysis and Sample Size Software (PASS
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Moreover, regulatory hurdles and integration into existing clinical workflows must be addressed
