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Trial · NCT03203850

Results by group132

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

OutcomeGroupCategoryValueSpreadUnits
Proportion of Patients Achieving Target SF ≤ 100 μg/L for the First TimeDeferasirox FCT 7mg/kgResponder4095% Confidence Interval 22.7 to 59.4percentage of participants
Proportion of Patients Achieving Target SF ≤ 100 μg/L for the First TimePhlebotomyResponder8095% Confidence Interval 51.9 to 95.7percentage of participants
Proportion of Patients Achieving Target SF ≤ 100 μg/L for the First TimeDeferasirox FCT 7mg/kgNon-Responder6095% Confidence Interval 40.6 to 77.3percentage of participants
Proportion of Patients Achieving Target SF ≤ 100 μg/L for the First TimePhlebotomyNon-Responder2095% Confidence Interval 4.3 to 48.1percentage of participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs)Deferasirox FCT 7mg/kgAt least one ocular AE9Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs)PhlebotomyAt least one ocular AE0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs)Deferasirox FCT 7mg/kgTreatment-related ocular AEs2Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs)PhlebotomyTreatment-related ocular AEs0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgCataract nuclear2Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyCataract nuclear0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgGlaucoma2Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyGlaucoma0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgBlepharitis1Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyBlepharitis0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgCellulitis orbital1Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyCellulitis orbital0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgDry eye1Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyDry eye0Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermDeferasirox FCT 7mg/kgEye pain1Participants
Number of Participants With Ocular Treatment Emergent Adverse Events (AEs) by Preferred TermPhlebotomyEye pain0Participants

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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