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Clinical Trial Summary

Observational cross-sectional multicenter study about effectiveness of two different sensor augmented-pumps with low glucose predictive function in Type 1 Diabetes Mellitus (T1DM) adult patients in routine clinical practice.


Clinical Trial Description

Cross-sectional multicenter analysis about clinical effectiveness of two different sensor-augmented pumps, Tandem T Slim X2 with Basal IQ (TTSX2) and Medtronic Minimed 640G with Smartguard (MM640G) in adult patients with type 1 Diabetes mellitus. All clinical variables are gathered from three EMR softwares and two sensor-augmented pumps sotwares. Data analysis is conducted using SPSS (Chicago, IL) statistics software. Results are presented as mean ± SD values or percentages. A Kruskal-Wallis or a Friedman test were used for the analysis of differences. Comparisons between proportions were analyzed using a chi-squared test. A "P" value < 0.05 was considered statistically significant. The protocol was approved by the reference Castilla-La Mancha Public Health Institute Ethic Committee. All participants provided written informed consent. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04741685
Study type Observational [Patient Registry]
Source Castilla-La Mancha Health Service
Contact
Status Completed
Phase
Start date February 15, 2021
Completion date June 10, 2021

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