ConductScience.org, home

Trial · NCT01473602

Results by group38

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With No Revision Surgery at 12 Months After Internal Fixation of a Low-Trauma Femoral Neck FractureTeriparatide7490% Confidence Interval 51 to 88Percentage of participants
Percentage of Participants With No Revision Surgery at 12 Months After Internal Fixation of a Low-Trauma Femoral Neck FracturePlacebo9390% Confidence Interval 70 to 99Percentage of participants
Percentage of Participants With Radiographic Evidence of HealingTeriparatide55.6Percentage of participants
Percentage of Participants With Radiographic Evidence of HealingPlacebo65.0Percentage of participants
Percentage of Participants With Pain Control During AmbulationTeriparatide90.0Percentage of participants
Percentage of Participants With Pain Control During AmbulationPlacebo100.0Percentage of participants
Percentage of Participants Without Severe Fracture-Site Pain During 24 Hours Prior to VisitTeriparatide81.8Percentage of participants
Percentage of Participants Without Severe Fracture-Site Pain During 24 Hours Prior to VisitPlacebo92.9Percentage of participants
Percentage of Participants Without Severe Fracture-Site Pain During Weight BearingTeriparatide90.9Percentage of participants
Percentage of Participants Without Severe Fracture-Site Pain During Weight BearingPlacebo84.6Percentage of participants
Percentage of Participants With Functional Evidence of HealingTeriparatide76.9Percentage of participants
Percentage of Participants With Functional Evidence of HealingPlacebo66.7Percentage of participants
Percentage of Participants Able to AmbulateTeriparatide76.9Percentage of participants
Percentage of Participants Able to AmbulatePlacebo93.3Percentage of participants
Percentage of Participants Who Regained Their Prefracture Ambulatory StatusTeriparatide47.1Percentage of participants
Percentage of Participants Who Regained Their Prefracture Ambulatory StatusPlacebo62.5Percentage of participants
Mean Change From Baseline to 6 Months in Worst Fracture-Site PainTeriparatideDuring ambulation ( n= 10, 13)-1.6Standard Error 1.46Units on a scale
Mean Change From Baseline to 6 Months in Worst Fracture-Site PainPlaceboDuring ambulation ( n= 10, 13)-1.3Standard Error 1.45Units on a scale
Mean Change From Baseline to 6 Months in Worst Fracture-Site PainTeriparatideDuring 24 hours preceding visit (n= 10, 14)-1.2Standard Error 1.27Units on a scale
Mean Change From Baseline to 6 Months in Worst Fracture-Site PainPlaceboDuring 24 hours preceding visit (n= 10, 14)-1.4Standard Error 1.21Units on a scale

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/NCT01473602/results