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Trial · NCT03301285

Registered outcomes12

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryChange from baseline (before start of zoledronic acid treatment) lumbar bone densitythrough study completion, 4 yearsreported in Z-score
SecondaryAgeBaseline
SecondarySexBaseline
SecondaryHeightBaseline
SecondaryWeightBaseline
SecondaryOccurrence of bone fracturesUntil baseline
SecondaryLong-term administration of vitamin/calcium supplement or notbaseline
SecondaryAdministration of drugs or notbaseline
SecondaryNumber of fractures after the start of zoledronic acid treatmentthrough study completion, 4 years
SecondaryChange from baseline phosphocalcic profile evaluationthrough study completion, 4 years
SecondaryFrequency of side effectsthrough study completion, 4 years
SecondaryChange from baseline lumbar bone density in sub-population of children with Rett syndrome after 1 year of zoledronic acid treatment1 year from baseline

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

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03301285/registered