ConductScience.org, home

Trial · NCT01455181

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Subjects Who Achieved the Primary Triple Endpoint at Week 24, Based on Investigator Prescribed Data.NPSP55875.095% Confidence Interval 53.3 to 90.2percentage of participants
Mean Percentage Changes From Baseline in Active Vitamin D Dosages at Each VisitNPSP558Week 2-47.08Standard Deviation 31.566percentage of change
Mean Percentage Changes From Baseline in Active Vitamin D Dosages at Each VisitNPSP558Week 4-80.38Standard Deviation 16.688percentage of change
Mean Percentage Changes From Baseline in Active Vitamin D Dosages at Each VisitNPSP558Week 8-96.70Standard Deviation 7.865percentage of change
Mean Percentage Changes From Baseline in Active Vitamin D Dosages at Each VisitNPSP558Week 16-96.18Standard Deviation 11.521percentage of change
Mean Percentage Changes From Baseline in Active Vitamin D Dosages at Each VisitNPSP558Week 24-97.92Standard Deviation 10.206percentage of change
Mean Percentage Changes From Baseline in Oral Calcium at Each VisitNPSP558Week 2-8.3Standard Deviation 36.20percentage of change
Mean Percentage Changes From Baseline in Oral Calcium at Each VisitNPSP558Week 4-46.4Standard Deviation 35.57percentage of change
Mean Percentage Changes From Baseline in Oral Calcium at Each VisitNPSP558Week 8-71.5Standard Deviation 33.14percentage of change
Mean Percentage Changes From Baseline in Oral Calcium at Each VisitNPSP558Week 16-71.7Standard Deviation 38.60percentage of change
Mean Percentage Changes From Baseline in Oral Calcium at Each VisitNPSP558Week 24-76.0Standard Deviation 40.48percentage of change
Proportion of Patients Achieving the Primary Endpoint at Each VisitNPSP558Week 220.8percentage of participants
Proportion of Patients Achieving the Primary Endpoint at Each VisitNPSP558Week 450.0percentage of participants
Proportion of Patients Achieving the Primary Endpoint at Each VisitNPSP558Week 870.8percentage of participants
Proportion of Patients Achieving the Primary Endpoint at Each VisitNPSP558Week 1683.3percentage of participants
Proportion of Patients Achieving the Primary Endpoint at Each VisitNPSP558Week 2483.3percentage of participants
Mean Change From Baseline in 24-hour Urine Calcium ExcretionNPSP558Week 8-64.58Standard Deviation 188.42mg/24 hour
Mean Change From Baseline in 24-hour Urine Calcium ExcretionNPSP558Week 24-51.53Standard Deviation 183.41mg/24 hour

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

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01455181/results