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Trial · NCT01831791

Results by group276

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Any Adverse Events (AEs) and Any Serious Adverse Events (SAEs)Dutasteride 0.5 mgAny AE64Participants
Number of Participants With Any Adverse Events (AEs) and Any Serious Adverse Events (SAEs)Dutasteride 0.5 mgAny SAE2Participants
Number of Participants With Drug-related, Treatment-emergent AEs and AE Leading to Premature Study Drug Discontinuation and Possible Suicidality-related Adverse Event (PSRAE)Dutasteride 0.5 mgAny drug related AEs20Participants
Number of Participants With Drug-related, Treatment-emergent AEs and AE Leading to Premature Study Drug Discontinuation and Possible Suicidality-related Adverse Event (PSRAE)Dutasteride 0.5 mgAny treatment-emergent AEs64Participants
Number of Participants With Drug-related, Treatment-emergent AEs and AE Leading to Premature Study Drug Discontinuation and Possible Suicidality-related Adverse Event (PSRAE)Dutasteride 0.5 mgAny AE leading to study drug discontinuation0Participants
Number of Participants With Drug-related, Treatment-emergent AEs and AE Leading to Premature Study Drug Discontinuation and Possible Suicidality-related Adverse Event (PSRAE)Dutasteride 0.5 mgAny PSRAE3Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgPBT, Change from N at BL to Y, n=1200Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgPBT, CS, Y (among change from N at BL to Y), n=00Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgPBT, CS, N (among change from N at BL to Y), n=00Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgNT, Change from N at BL to Y, n=1201Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgNT, CS, Y (among change from N at BL to Y), n=11Participants
Number of Participants With Change From Baseline in Breast Examination Results Any Time Post-Baseline VisitDutasteride 0.5 mgNT, CS, N (among change from N at BL to Y), n=00Participants
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgHemoglobin, Week 26, n=1140.61Standard Deviation 5.891Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgHemoglobin, Week 52, n=111-0.94Standard Deviation 5.657Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgHemoglobin, Final value, n=118-0.69Standard Deviation 5.792Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgAlbumin, Week 26, n=114-0.64Standard Deviation 2.014Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgAlbumin, Week 52, n=111-1.42Standard Deviation 1.928Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgAlbumin, Final value, n=118-1.31Standard Deviation 1.969Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgTotal protein, Week 26, n=114-0.17Standard Deviation 3.741Grams per liter (g/L)
Mean Change From Baseline in Hemoglobin, Albumin and Total Protein at the Indicated Time PointsDutasteride 0.5 mgTotal protein, Week 52, n=111-0.55Standard Deviation 3.389Grams per liter (g/L)

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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