Condition: Type 1 Diabetes (T1D) · Sponsor: Sue Brown
This study is a randomized cross-over trial comparing AIDANET with Anticipation to AIDANET in FCL without Anticipation. Participants will complete 4 weeks of AID data collection which will be used to establish baseline and initialize the control algorithm. Participants will then be randomized to one of two groups: Group A: AIDANET in FCL with Anticipation (AIDANET+ACL), and Group B: AIDANET in FCL without Anticipation (AIDANET+FCL). The study duration of each group is 4 weeks each. The order of these two phases will be dependent upon randomization.
This description comes directly from the study's public registry record.
Andrea Riana, MD · (434) 249-6251 · rys6hm@uvahealth.org
Laura Kollar, RN · (434) 982-6479 · llk7m@uvahealth.org
Always discuss trial participation with your own doctor first.
| University of Virginia Center for Diabetes Technology | Charlottesville, Virginia, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07507708