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. 2019 Jul 4;16(4):385–395. doi: 10.1177/1479164119827456

Figure 1.

Figure 1.

Trial design. Following consent, screening and enrolment, all participants had a professional flash sensor applied to the upper arm for the 14-day baseline period. Participants with baseline sensor data of ⩾500 sensor glucose readings were randomised to one of the three study groups as shown.