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Trial · NCT03574597

Results by group60

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

OutcomeGroupCategoryValueSpreadUnits
Participants From Time of Randomisation to First Occurrence of HF Requiring Hospitalisation or Urgent HF VisitSemaglutide97Participants
Participants From Time of Randomisation to First Occurrence of HF Requiring Hospitalisation or Urgent HF VisitPlacebo122Participants
Participants From Time of Randomisation to First Occurrence of Glycosylated Haemoglobin (HbA1c) Greater Than Equals to (≥) 48 Millimole Per Mole (mmol/Mol) (6.5 Percentage [%])Semaglutide306Participants
Participants From Time of Randomisation to First Occurrence of Glycosylated Haemoglobin (HbA1c) Greater Than Equals to (≥) 48 Millimole Per Mole (mmol/Mol) (6.5 Percentage [%])Placebo1059Participants
Participants From Time of Randomisation to First Occurrence of a 5-component Composite Nephropathy Outcome MeasureSemaglutide155Participants
Participants From Time of Randomisation to First Occurrence of a 5-component Composite Nephropathy Outcome MeasurePlacebo198Participants
Participants From Time of Randomisation to HbA1c ≥ 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c <39 mmol/Mol [5.7%])Semaglutide623Participants
Participants From Time of Randomisation to HbA1c ≥ 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c <39 mmol/Mol [5.7%])Placebo1501Participants
Participants With HbA1c < 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c ≥ 39 mmol/Mol [5.7%])SemaglutideWeek 523363Participants
Participants With HbA1c < 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c ≥ 39 mmol/Mol [5.7%])PlaceboWeek 52955Participants
Participants With HbA1c < 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c ≥ 39 mmol/Mol [5.7%])SemaglutideWeek 1043271Participants
Participants With HbA1c < 39 mmol/Mol (5.7%) (for Participants With a Screening HbA1c ≥ 39 mmol/Mol [5.7%])PlaceboWeek 104978Participants
Change in Systolic Blood Pressure (SBP)Semaglutide-3.8Standard Deviation 16.4Millimetre of mercury (mmHg)
Change in Systolic Blood Pressure (SBP)Placebo-0.6Standard Deviation 16.0Millimetre of mercury (mmHg)
Change in Diastolic Blood Pressure (DBP)Semaglutide-1.1Standard Deviation 10.4mmHg
Change in Diastolic Blood Pressure (DBP)Placebo-0.4Standard Deviation 10.4mmHg
Change in PulseSemaglutide3.8Standard Deviation 11.0beats per mintue (bpm)
Change in PulsePlacebo0.9Standard Deviation 10.7beats per mintue (bpm)
Change in High Sensitivity C-Reactive Protein (hsCRP) - Ratio to BaselineSemaglutide0.61Geometric Coefficient of Variation 149.53ratio of hsCRP
Change in High Sensitivity C-Reactive Protein (hsCRP) - Ratio to BaselinePlacebo1.00Geometric Coefficient of Variation 133.25ratio of hsCRP

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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