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Trial · NCT01971164

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryNumber of subjects with adverse events15 days
PrimaryVital signs and 12 lead ECGs15 days
PrimaryCmax (maximum concentration)15 days
Primarytmax (time to reach maximum concentration)15 days
Primaryt1/2 (elimination half-life)15 days
PrimaryAUC (area under the concentration-time curve)15 days
PrimaryAR (accumulation ratio)15 days
PrimaryRBC (red blood cell) count15 days
PrimaryHgb (hemoglobin)15 days
PrimaryTSAT (transferrin saturation)15 days
Primaryserum ferritin15 days

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.

For software

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GET https://conductscience.org/api/trials/v1/NCT01971164/registered