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Comparison · NCT01705587-35bd4a02

Immediate Teriparatide vs Delayed Teriparatide: Radiologic Evidence of Healing

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Immediate Teriparatide vs Delayed Teriparatide: Radiologic Evidence of Healing. Trial comparisons, record NCT01705587-35bd4a02. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01705587-35bd4a02

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 110.5661wilson
Risk in group 210.511wilson
Risk difference, group 1 minus group 20-0.4340.49newcombe hybrid score
Risk ratio, group 1 over group 2111log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treatfrom the risk difference intervalthe two groups' risks are equal

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Immediate TeriparatideOpen label teriparatide given immediately following surgical repair of fracture~teriparatide: 20 microgram once-daily subcutaneous injection55OG000
Group 2Delayed TeriparatideOpen label teriparatide given six months following surgical repair of fracture~teriparatide: 20 microgram once-daily subcutaneous injection44OG001

Outcome

Type
PRIMARY
Title
Radiologic Evidence of Healing
Description
Number of participants with persistence of alignment as determined by a radiologist.
Time frame
at 10 weeks for immediate teriparatide group
Population
Based on orthopedic surgeons' assessment, x-rays were not deemed necessary in over 30% of patients at week 10. Results presented are for those who had x-rays at 10 weeks to assess persistence of alignment for safety purposes.

Source ClinicalTrials.gov

Trial

Title
Fracture (FX) Improvement With Teriparatide: FiX-IT Study
NCT number
NCT01705587
Phases
PHASE4
Conditions
Osteoporosis, Atypical Femoral Fracture
Interventions
teriparatide
Lead sponsor
Susan L. Greenspan
Results first posted
2017-12-12

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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