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Trial · NCT05691257

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange in the hemoglobin from baselineup to 8 weekHemoglobin is calculated by the routine blood test
SecondaryChange in N-terminal Pro-brain Natriuretic Peptide (NT-proBNP)Up to 8 weeks
Change from baseline to week 12 in N-terminal pro-brain natriuretic peptide (NT-proBNP). Baseline value was defined as the mean of all available measurements from the screening visit until start of treatment with randomised study medication.
SecondaryChange in Left Ventricular Systolic FunctionUp to 24 weeksChange in left ventricular ejection fraction is assessed by two-dimensional directed M-mode echocardiography
SecondaryChange in Left Ventricular End-Diastolic DiameterUp to 24 weeksChange in left ventricular end-diastolic diameter is assessed by two-dimensional directed M-mode echocardiography
SecondaryChange in Left Ventricular Diastolic FunctionUp to 24 weeksChange in E/e' is assessed by two-dimensional directed M-mode echocardiography
SecondaryChange in Low-density lipoprotein(LDL)Up to 8 weeks
Change from baseline to week 8 in Low-density lipoprotein(LDL).Baseline value was defined as the mean of all available measurements from the screening visit until start of treatment with randomised study medication.
SecondaryChange in Serum ferritinUp to 8 weeks
Change from baseline to week 8 in Serum ferritin.Baseline value was defined as the mean of all available measurements from the screening visit until start of treatment with randomised study medication.
SecondaryChange in Transferrin saturationUp to 8 weeks
Change from baseline to week 8 in Transferrin saturation.Baseline value was defined as the mean of all available measurements from the screening visit until start of treatment with randomised study medication.
SecondaryChange in Left atrial volumeUp to 24 weeksChange in left atrial volume is assessed by two-dimensional directed M-mode echocardiography
SecondaryChange in Left atrial volume indexUp to 24 weeksChange in left atrial volume index is assessed by two-dimensional directed M-mode echocardiography
OtherLiver InjuryUp to 8 weeks
Liver injury is defined as: i) a rise of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) to 3 times above the upper limit of normal \[ULN\], or ii) a rise of total bilirubin to 2 times above the upper limit of normal \[ULN\]
OtherHyperkalemiaUp to 8 weeksHyperkalemia is defined as:Serum potassium \> 5.5 mmol/L
OtherThromboembolismUp to 1 yearThromboembolism is defined as:Deep vein thrombosis at follow-up

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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GET https://conductscience.org/api/trials/v1/NCT05691257/registered