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Trial · NCT02780141

Registered outcomes28

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

ListOutcomeTime frameDescription
PrimaryHemoglobin (Hb) Response rateUp to Week 24Hb response is defined as reaching target values for Hb and change of Hb from baseline
SecondaryAverage Hb level from Week 18 to 24Week 18 to 24
SecondaryChange from baseline in the average Hb level from Week 18 to 24Baseline and Weeks 18 to 24
SecondaryProportion of participants with the target Hb level from Week 18 to 24Week 18 to 24
SecondaryRate of rise in Hb levels (g/dL/week) from week 0 to at the earliest date of week 4, time of discontinuation, or time of dose adjustmentUp to Week 4
SecondaryProportion of measurement points with the target Hb levelUp to Week 24
SecondaryProportion of participants with the target Hb level at each weekUp to Week 24
SecondaryProportion of participants with the lower limit of the target Hb levelUp to Week 24
SecondaryTime to achieve the lower limit of the target Hb levelUp to Week 24
SecondaryChange from baseline in Hb levels to each weekBaseline and Up to Week 24
SecondaryAverage hematocrit levelUp to Week 24
SecondaryAverage reticulocyte levelUp to Week 24
SecondaryAverage iron (Fe) levelUp to Week 24
SecondaryAverage ferritin levelUp to Week 24
SecondaryAverage transferrin levelUp to Week 24
SecondaryAverage total iron binding capacity levelUp to Week 24
SecondaryAverage soluble transferrin receptor levelUp to Week 24
SecondaryAverage transferrin saturation levelUp to Week 24
SecondaryAverage reticulocyte hemoglobin content levelUp to Week 24
SecondaryQuality of life assessed by EQ-5D-5LUp to Week 24EQ-5D-5L: EuroQol 5 Dimension 5 Levels

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/NCT02780141/registered