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Our plan to conduct sensitivity or subgroup analyses based on risk-of-bias assessment, trial duration and background glucose-lowering treatment was also not implemented

10.1172/jci.insight.140532 46 XiaT.HeW.LuoZ.WangK.TanX

doi: 10.1093/icvts/ivy163 25 Sciences CfIOoM

Some patients benefit from slower escalation, extended time at intermediate doses, or dose reduction if side effects are intolerable