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Clinical Trial Details

Trial ID: L6587
Source ID: NCT05882071
Associated Drug: Sodium/Glucose Cotransporter-2 Inhibitors (Sglt2i)
Title: Non-interventional Study (NIS) on Sodium-glucose Co-transporter-2 Inhibitors (SGLT2i) Use in France
Acronym:
Status: ACTIVE_NOT_RECRUITING
Study Results: NO
Results:
Conditions: Diabetes Mellitus, Type 2
Interventions: DRUG: Sodium/glucose cotransporter-2 inhibitors (SGLT2i)
Outcome Measures: Primary: Baseline characteristic: Age, up to 5 years|Baseline characteristic: Gender, up to 5 years|Baseline characteristic: Region of residence, up to 5 years|Baseline characteristic: History of diabetes (date of first Long Term Disease (LTD) status related to diabetes), up to 5 years|Baseline characteristic: Type of diabetes, up to 5 years|Proportion of patients with a history of cardio-vascular events including heart failure hospitalizations and lower limb amputation, renal events, ketoacidosis, Fournier's gangrene over the two years before the index date (initiation of SGLT2i), up to 5 years | Secondary: Incidence rate of acute cardiovascular atheromatous events during the exposure period following initiation of the SGLT2i, up to 5 years|Time from drug initiation to first event of acute cardiovascular atheromatous events, up to 5 years|Incidence rate of heart failure hospitalization during the exposure period following initiation of the SGLT2i, up to 5 years|Time from drug initiation to first event of heart failure hospitalization, up to 5 years|Incidence rate of deaths all cause during the exposure period following initiation of the SGLT2i, up to 5 years|Time from drug initiation to death all cause, up to 5 years
Sponsor/Collaborators: Sponsor: Boehringer Ingelheim
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases:
Enrollment: 547150
Study Type: OBSERVATIONAL
Study Designs: Observational Model: |Time Perspective: p
Start Date: 2023-11-15
Completion Date: 2026-07-31
Results First Posted:
Last Update Posted: 2024-11-27
Locations: Boehringer Ingelheim, Paris, 75013, France
URL: https://clinicaltrials.gov/show/NCT05882071