<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carlson AL</submitter><funding>NIDDK NIH HHS</funding><pagination>178-189</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8971997</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(3)</volume><pubmed_abstract>&lt;b>&lt;i>Introduction:&lt;/i>&lt;/b> This trial assessed safety and effectiveness of an advanced hybrid closed-loop (AHCL) system with automated basal (Auto Basal) and automated bolus correction (Auto Correction) in adolescents and adults with type 1 diabetes (T1D). &lt;b>&lt;i>Materials and Methods:&lt;/i>&lt;/b> This multicenter single-arm study involved an intent-to-treat population of 157 individuals (39 adolescents aged 14-21 years and 118 adults aged ≥22-75 years) with T1D. Study participants used the MiniMed™ AHCL system during a baseline run-in period in which sensor-augmented pump +/- predictive low glucose management or Auto Basal was enabled for ∼14 days. Thereafter, Auto Basal and Auto Correction were enabled for a study phase (∼90 days), with glucose target set to 100 or 120 mg/dL for ∼45 days, fo</pubmed_abstract><journal>Diabetes technology &amp; therapeutics</journal><pubmed_title>Safety and Glycemic Outcomes During the MiniMed™ Advanced Hybrid Closed-Loop System Pivotal Trial in Adolescents and Adults with Type 1 Diabetes.</pubmed_title><pmcid>PMC8971997</pmcid><funding_grant_id>P30 DK045735</funding_grant_id><funding_grant_id>P30 DK020572</funding_grant_id><funding_grant_id>P30 DK111022</funding_grant_id><pubmed_authors>Kipnes MS</pubmed_authors><pubmed_authors>Shin J</pubmed_authors><pubmed_authors>Vella M</pubmed_authors><pubmed_authors>Slover RH</pubmed_authors><pubmed_authors>Sherr JL</pubmed_authors><pubmed_authors>Christiansen M</pubmed_authors><pubmed_authors>Grosman B</pubmed_authors><pubmed_authors>Lilenquist DR</pubmed_authors><pubmed_authors>Thrasher JR</pubmed_authors><pubmed_authors>Cordero TL</pubmed_authors><pubmed_authors>Jonkers RAM</pubmed_authors><pubmed_authors>Rhinehart AS</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Kaiserman KB</pubmed_authors><pubmed_authors>Vigersky RA</pubmed_authors><pubmed_authors>Shulman DI</pubmed_authors><pubmed_authors>Carlson AL</pubmed_authors><pubmed_authors>Pop-Busui R</pubmed_authors><pubmed_authors>Roy A</pubmed_authors><pubmed_authors>Bode BW</pubmed_authors><pubmed_authors>Lee SW</pubmed_authors><pubmed_authors>Reed JHC</pubmed_authors><pubmed_authors>Brazg RL</pubmed_authors><pubmed_authors>Philis-Tsimikas A</pubmed_authors><pubmed_authors>Garg SK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and Glycemic Outcomes During the MiniMed™ Advanced Hybrid Closed-Loop System Pivotal Trial in Adolescents and Adults with Type 1 Diabetes.</name><description>&lt;b>&lt;i>Introduction:&lt;/i>&lt;/b> This trial assessed safety and effectiveness of an advanced hybrid closed-loop (AHCL) system with automated basal (Auto Basal) and automated bolus correction (Auto Correction) in adolescents and adults with type 1 diabetes (T1D). &lt;b>&lt;i>Materials and Methods:&lt;/i>&lt;/b> This multicenter single-arm study involved an intent-to-treat population of 157 individuals (39 adolescents aged 14-21 years and 118 adults aged ≥22-75 years) with T1D. Study participants used the MiniMed™ AHCL system during a baseline run-in period in which sensor-augmented pump +/- predictive low glucose management or Auto Basal was enabled for ∼14 days. Thereafter, Auto Basal and Auto Correction were enabled for a study phase (∼90 days), with glucose target set to 100 or 120 mg/dL for ∼45 days, fo</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-04T12:45:21.389Z</modification><creation>2025-04-04T12:45:21.389Z</creation></dates><accession>S-EPMC8971997</accession><cross_references><pubmed>34694909</pubmed><doi>10.1089/dia.2021.0319</doi></cross_references></HashMap>