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Trial · NCT01453049

Results by group150

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 24Rosiglitazone+Glimepiride FDC-1.75Standard Deviation 1.078Percent of total hemoglobin
Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 24Glimepiride-1.47Standard Deviation 1.227Percent of total hemoglobin
Change From Baseline in Fasting Plasma Glucose (FPG) at Week 24Rosiglitazone+Glimepiride FDC-1.907Standard Deviation 2.9601Millimoles per liter (mmol/L)
Change From Baseline in Fasting Plasma Glucose (FPG) at Week 24Glimepiride-0.877Standard Deviation 2.0673Millimoles per liter (mmol/L)
Number of HbA1c Responders and Non-respondersRosiglitazone+Glimepiride FDCResponders33participants
Number of HbA1c Responders and Non-respondersGlimepirideResponders29participants
Number of HbA1c Responders and Non-respondersRosiglitazone+Glimepiride FDCNon-responders2participants
Number of HbA1c Responders and Non-respondersGlimepirideNon-responders9participants
Number of FPG Responders and Non-respondersRosiglitazone+Glimepiride FDCResponders21participants
Number of FPG Responders and Non-respondersGlimepirideResponders12participants
Number of FPG Responders and Non-respondersRosiglitazone+Glimepiride FDCNon-responders14participants
Number of FPG Responders and Non-respondersGlimepirideNon-responders26participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineRosiglitazone+Glimepiride FDCHbA1c <7%13participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineGlimepirideHbA1c <7%13participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineRosiglitazone+Glimepiride FDCHbA1c <=6.5%5participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineGlimepirideHbA1c <=6.5%8participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineRosiglitazone+Glimepiride FDCHbA1c decrease of >=0.7% from Baseline33participants
Number of Participants Who Achieved HbA1c <7%, HbA1c <=6.5%, or Who Achieved a Decrease of >=0.7% From BaselineGlimepirideHbA1c decrease of >=0.7% from Baseline29participants
Change From Baseline in Fasting Proinsulin and Insulin at Week 24/Early Withdrawal (EW)Rosiglitazone+Glimepiride FDCProinsulin; n=32, 34-2.9Standard Deviation 10.18Picomoles per liter (pmol/L)
Change From Baseline in Fasting Proinsulin and Insulin at Week 24/Early Withdrawal (EW)GlimepirideProinsulin; n=32, 343.1Standard Deviation 10.70Picomoles per liter (pmol/L)

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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