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Trial · NCT03000673

Results by group340

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

OutcomeGroupCategoryValueSpreadUnits
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment BAdverse Events4Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment CAdverse Events4Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment DAdverse Events3Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment AAdverse Events2Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment BSerious Adverse Events0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment CSerious Adverse Events0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment DSerious Adverse Events0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment ASerious Adverse Events0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment BAdverse Events Leading to Discontinuations0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment CAdverse Events Leading to Discontinuations0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment DAdverse Events Leading to Discontinuations0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment AAdverse Events Leading to Discontinuations0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment BDeaths0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment CDeaths0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment DDeaths0Participants
The Number of Adverse Events (AEs), Serious AEs (SAEs), AEs Leading to Discontinuation and DeathTreatment ADeaths0Participants
The Number of Participants Marked Abnormalities in Clinical Laboratory Tests : Hematology I; Hematology II; CoagulationTreatment BHematology I Hemoglobin (G/DL) Abnormal low3Participants
The Number of Participants Marked Abnormalities in Clinical Laboratory Tests : Hematology I; Hematology II; CoagulationTreatment CHematology I Hemoglobin (G/DL) Abnormal low3Participants
The Number of Participants Marked Abnormalities in Clinical Laboratory Tests : Hematology I; Hematology II; CoagulationTreatment DHematology I Hemoglobin (G/DL) Abnormal low2Participants
The Number of Participants Marked Abnormalities in Clinical Laboratory Tests : Hematology I; Hematology II; CoagulationTreatment AHematology I Hemoglobin (G/DL) Abnormal low1Participants

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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