IDegLira
DrugCollecting data reported in medical records of patients with T2D, who had initiated treatment with commercially available IDegLira according to the routine clinical practice and local label at the discretion of the treating physician
NCT Number: NCT05324462
The purpose of this study is to investigate the glycaemic control and other clinical parameters in adult patients previously treated with basal insulin (with or without OADs) and switched to IDegLira in real-world clinical practice in Colombia.
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Notify Me18 year and older
All sexes
Observational
Novo Nordisk Investigational Site, Medellín, Antioquia, Colombia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Collecting data reported in medical records of patients with T2D, who had initiated treatment with commercially available IDegLira according to the routine clinical practice and local label at the discretion of the treating physician
Time frame: From baseline (week 0) to end of study (week 26 plus/minus 6 weeks) after IDegLira initiation
Percentage point
Time frame: From baseline (week 0) to end of study (week 26 plus/minus 6 weeks) after IDegLira initiation
Kilogram (kg)
Time frame: From baseline (week 0) to end of study (week 26 plus/minus 6 weeks) after IDegLira initiation
Units/day
Novo Nordisk A/S
Industry
Glycaemic Control and Other Clinical Parameters in Adult Type 2 Diabetes Patients on Basal Insulin Initiating Treatment With IDegLira in Routine Clinical Practice in Colombia - A Single-arm, Non-interventional Retrospective Chart Review Study
Acronym: SPIRIT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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