Design of clinical trials to assess diabetes treatment: Minimum duration of continuous glucose monitoring data to estimate time-in-ranges with the desired precision.

Nunzio CamerlingoMartina VettorettiGiovanni SparacinoAndrea FacchinettiJulia Katharina MaderPratik ChoudharySimone Del Faveronull null
Published in: Diabetes, obesity & metabolism (2021)
The presented approach can be used to both compute the uncertainty of time-in-ranges and determine the minimum duration of a trial to achieve the desired precision. An online tool to facilitate its implementation is made freely available to the clinical investigator.