<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Brown SA</submitter><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><pagination>1822-1828</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7372060</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(8)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Limited information is available about glycemic outcomes with a closed-loop control (CLC) system compared with a predictive low-glucose suspend (PLGS) system.&lt;h4>Research design and methods&lt;/h4>After 6 months of use of a CLC system in a randomized trial, 109 participants with type 1 diabetes (age range, 14-72 years; mean HbA&lt;sub>1c&lt;/sub>, 7.1% [54 mmol/mol]) were randomly assigned to CLC (&lt;i>N&lt;/i> = 54, Control-IQ) or PLGS (&lt;i>N&lt;/i> = 55, Basal-IQ) groups for 3 months. The primary outcome was continuous glucose monitor (CGM)-measured time in range (TIR) for 70-180 mg/dL. Baseline CGM metrics were computed from the last 3 months of the preceding study.&lt;h4>Results&lt;/h4>All 109 participants completed the study. Mean ± SD TIR was 71.1 ± 11.2% at baseline and 67.6 ± 12.6% using</pubmed_abstract><journal>Diabetes care</journal><pubmed_title>Glycemic Outcomes of Use of CLC Versus PLGS in Type 1 Diabetes: A Randomized Controlled Trial.</pubmed_title><pmcid>PMC7372060</pmcid><funding_grant_id>P30 DK036836</funding_grant_id><funding_grant_id>UC4 DK108483</funding_grant_id><funding_grant_id>UC4 108483</funding_grant_id><pubmed_authors>McCrady-Spitzer S</pubmed_authors><pubmed_authors>Willi SM</pubmed_authors><pubmed_authors>Levy CJ</pubmed_authors><pubmed_authors>Patibandla N</pubmed_authors><pubmed_authors>Eggerman T</pubmed_authors><pubmed_authors>Slover R</pubmed_authors><pubmed_authors>Laffel LM</pubmed_authors><pubmed_authors>Anderson SM</pubmed_authors><pubmed_authors>Dadlani V</pubmed_authors><pubmed_authors>Isganaitis E</pubmed_authors><pubmed_authors>Forlenza G</pubmed_authors><pubmed_authors>Flint E</pubmed_authors><pubmed_authors>Tabatabai I</pubmed_authors><pubmed_authors>Beck R</pubmed_authors><pubmed_authors>Beck RW</pubmed_authors><pubmed_authors>Calvo K</pubmed_authors><pubmed_authors>Simha V</pubmed_authors><pubmed_authors>Brown SA</pubmed_authors><pubmed_authors>Legault L</pubmed_authors><pubmed_authors>Ambler-Osborn L</pubmed_authors><pubmed_authors>Levister C</pubmed_authors><pubmed_authors>Renard E</pubmed_authors><pubmed_authors>Keller J</pubmed_authors><pubmed_authors>Berget C</pubmed_authors><pubmed_authors>Pinsker JE</pubmed_authors><pubmed_authors>Andre C</pubmed_authors><pubmed_authors>Murphy C</pubmed_authors><pubmed_authors>Kollman C</pubmed_authors><pubmed_authors>Campos T</pubmed_authors><pubmed_authors>iDCL Trial Research Group</pubmed_authors><pubmed_authors>Emory E</pubmed_authors><pubmed_authors>Jost E</pubmed_authors><pubmed_authors>Jacobson T</pubmed_authors><pubmed_authors>Gabrielson D</pubmed_authors><pubmed_authors>Breton MD</pubmed_authors><pubmed_authors>Conshafter K</pubmed_authors><pubmed_authors>Kovatchev B</pubmed_authors><pubmed_authors>O'Malley G</pubmed_authors><pubmed_authors>Castle J</pubmed_authors><pubmed_authors>Lam D</pubmed_authors><pubmed_authors>Doyle Iii F</pubmed_authors><pubmed_authors>Kudva YC</pubmed_authors><pubmed_authors>Reznik Y</pubmed_authors><pubmed_authors>Anderson S</pubmed_authors><pubmed_authors>Kim K</pubmed_authors><pubmed_authors>Levy C</pubmed_authors><pubmed_authors>Rossick-Solis A</pubmed_authors><pubmed_authors>Raghinaru D</pubmed_authors><pubmed_authors>Borgman S</pubmed_authors><pubmed_authors>Kovatchev BP</pubmed_authors><pubmed_authors>Laffel L</pubmed_authors><pubmed_authors>Pinsker J</pubmed_authors><pubmed_authors>Ekhlaspour L</pubmed_authors><pubmed_authors>Morris K</pubmed_authors><pubmed_authors>Dassau E</pubmed_authors><pubmed_authors>Lum JW</pubmed_authors><pubmed_authors>Wysham C</pubmed_authors><pubmed_authors>Towers L</pubmed_authors><pubmed_authors>Belle SH</pubmed_authors><pubmed_authors>Church MM</pubmed_authors><pubmed_authors>Salas E</pubmed_authors><pubmed_authors>Voelmle M</pubmed_authors><pubmed_authors>Messer L</pubmed_authors><pubmed_authors>Doyle F</pubmed_authors><pubmed_authors>Buckingham BA</pubmed_authors><pubmed_authors>Doyle FJ</pubmed_authors><pubmed_authors>Mitchell H</pubmed_authors><pubmed_authors>Roethke L</pubmed_authors><pubmed_authors>Piper M</pubmed_authors><pubmed_authors>Alonso GT</pubmed_authors><pubmed_authors>Buckingham B</pubmed_authors><pubmed_authors>Lum J</pubmed_authors><pubmed_authors>Wakeman C</pubmed_authors><pubmed_authors>Green J</pubmed_authors><pubmed_authors>Breton M</pubmed_authors><pubmed_authors>Ogyaadu S</pubmed_authors><pubmed_authors>Passman S</pubmed_authors><pubmed_authors>Green N</pubmed_authors><pubmed_authors>Forlenza GP</pubmed_authors><pubmed_authors>Cobelli C</pubmed_authors><pubmed_authors>Lovett J</pubmed_authors><pubmed_authors>Oliveri M</pubmed_authors><pubmed_authors>Gondor-Fredrick L</pubmed_authors><pubmed_authors>Town M</pubmed_authors><pubmed_authors>Arreza-Rubin G</pubmed_authors><pubmed_authors>Wadwa RP</pubmed_authors><pubmed_authors>Reid C</pubmed_authors><pubmed_authors>Kumari K</pubmed_authors><pubmed_authors>Brown S</pubmed_authors><pubmed_authors>Janicek R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glycemic Outcomes of Use of CLC Versus PLGS in Type 1 Diabetes: A Randomized Controlled Trial.</name><description>&lt;h4>Objective&lt;/h4>Limited information is available about glycemic outcomes with a closed-loop control (CLC) system compared with a predictive low-glucose suspend (PLGS) system.&lt;h4>Research design and methods&lt;/h4>After 6 months of use of a CLC system in a randomized trial, 109 participants with type 1 diabetes (age range, 14-72 years; mean HbA&lt;sub>1c&lt;/sub>, 7.1% [54 mmol/mol]) were randomly assigned to CLC (&lt;i>N&lt;/i> = 54, Control-IQ) or PLGS (&lt;i>N&lt;/i> = 55, Basal-IQ) groups for 3 months. The primary outcome was continuous glucose monitor (CGM)-measured time in range (TIR) for 70-180 mg/dL. Baseline CGM metrics were computed from the last 3 months of the preceding study.&lt;h4>Results&lt;/h4>All 109 participants completed the study. Mean ± SD TIR was 71.1 ± 11.2% at baseline and 67.6 ± 12.6% using</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Aug</publication><modification>2025-05-29T20:48:18.583Z</modification><creation>2022-02-11T02:08:12.753Z</creation></dates><accession>S-EPMC7372060</accession><cross_references><pubmed>32471910</pubmed><doi>10.2337/dc20-0124</doi></cross_references></HashMap>