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Trial · NCT02451137

Results by group104

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Individualized Glycated Hemoglobin Target Attainment Per Healthcare Effectiveness Data and Information Set (HEDIS) Criteria Without Documented Symptomatic(Blood Glucose <=70 mg/dL [<=3.9 mmol/L]) and/or Severe Hypoglycemia
Toujeo31.3percentage of participants
Percentage of Participants With Individualized Glycated Hemoglobin Target Attainment Per Healthcare Effectiveness Data and Information Set (HEDIS) Criteria Without Documented Symptomatic(Blood Glucose <=70 mg/dL [<=3.9 mmol/L]) and/or Severe Hypoglycemia
Standard of Care27.9percentage of participants
Change From Baseline in HbA1c at Month 6 and Month 12ToujeoMonth 6-1.40Standard Error 0.030percentage of HbA1c
Change From Baseline in HbA1c at Month 6 and Month 12Standard of CareMonth 6-1.36Standard Error 0.030percentage of HbA1c
Change From Baseline in HbA1c at Month 6 and Month 12ToujeoMonth 12-1.29Standard Error 0.034percentage of HbA1c
Change From Baseline in HbA1c at Month 6 and Month 12Standard of CareMonth 12-1.24Standard Error 0.034percentage of HbA1c
Treatment Persistence Measured by Medication Possession Ratio (MPR)ToujeoMonth 662.06Standard Deviation 26.98Medication Possession ratio
Treatment Persistence Measured by Medication Possession Ratio (MPR)Standard of CareMonth 663.14Standard Deviation 28.42Medication Possession ratio
Treatment Persistence Measured by Medication Possession Ratio (MPR)ToujeoMonth 1258.21Standard Deviation 28.87Medication Possession ratio
Treatment Persistence Measured by Medication Possession Ratio (MPR)Standard of CareMonth 1257.82Standard Deviation 29.97Medication Possession ratio
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <3.0 mmol/L (<54 mg/dL) and/or Severe Hypoglycemia During the 6-Month Randomized PeriodToujeo37.3percentage of participants
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <3.0 mmol/L (<54 mg/dL) and/or Severe Hypoglycemia During the 6-Month Randomized PeriodStandard of Care34.3percentage of participants
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <=3.9 mmol/L (<= 70 mg/dL) and <3.0 mmol/L (< 54 mg/dL) and/or Severe Hypoglycemia During the 12-Month Randomized Period
ToujeoMonth 12: <=70 mg/dL26.1percentage of participants
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <=3.9 mmol/L (<= 70 mg/dL) and <3.0 mmol/L (< 54 mg/dL) and/or Severe Hypoglycemia During the 12-Month Randomized Period
Standard of CareMonth 12: <=70 mg/dL23.7percentage of participants
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <=3.9 mmol/L (<= 70 mg/dL) and <3.0 mmol/L (< 54 mg/dL) and/or Severe Hypoglycemia During the 12-Month Randomized Period
ToujeoMonth 12: <54 mg/dL33.0percentage of participants
Percentage of Participants Reaching Individualized HbA1c Target Without Documented Symptomatic <=3.9 mmol/L (<= 70 mg/dL) and <3.0 mmol/L (< 54 mg/dL) and/or Severe Hypoglycemia During the 12-Month Randomized Period
Standard of CareMonth 12: <54 mg/dL29.5percentage of participants
Change From Baseline in Fasting Plasma Glucose (FPG) at Month 6 and Month 12ToujeoMonth 6-48.9Standard Error 1.56mg/dL
Change From Baseline in Fasting Plasma Glucose (FPG) at Month 6 and Month 12Standard of CareMonth 6-50.4Standard Error 1.58mg/dL
Change From Baseline in Fasting Plasma Glucose (FPG) at Month 6 and Month 12ToujeoMonth 12-48.0Standard Error 1.66mg/dL
Change From Baseline in Fasting Plasma Glucose (FPG) at Month 6 and Month 12Standard of CareMonth 12-47.3Standard Error 1.69mg/dL

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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