Adults 18 to 74, any sex, with Type1 Diabetes Mellitus. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
System SuitabilityPrimary· 36-48 hours
Technology Acceptance Questionnaire Score Scores are on a Likert Scale of 1-Not at All to 5-Extremely for Ease of Use, Usability and Trust in System Scores.
Ease of Use
Group
Value
95% CI
Tandem t:Slim X2 With Control-IQ Technology
5
5 – 5
Usefulness
Group
Value
95% CI
Tandem t:Slim X2 With Control-IQ Technology
4.8
4 – 5
Trust in System
Group
Value
95% CI
Tandem t:Slim X2 With Control-IQ Technology
5
5 – 5
Sponsor's own description
A 36-48 hour admission testing the t:slim X2 with Control-IQ Technology
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
Other trials of Tandem t:slim X2 with Control-IQ Technology
Trials testing the same drug.
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Other recruiting trials for Type1 Diabetes Mellitus
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Other University of Virginia trials
Trials by the same sponsor.
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Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
Sponsor: as reported to ClinicalTrials.gov by University of Virginia
Last refreshed: 25 May 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03368937.