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80.9 1.8 kg, p = 0.007) after carnitine supplementation for 4 weeks ( Randomization, blinding, and intervention Following a 2-week run-in period, the participants were randomly allocated to the L-carnitine + synbiotic or L-carnitine + placebo groups via block randomization in a 1:1 ratio, in blocks of two, stratified by age, using the Random Allocation Software (RAS)
When analyzing the association of carnitine with osteopenia, osteoporosis cases were excluded from the analysis