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Trial · NCT00533273

Registered outcomes18

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

ListOutcomeTime frameDescription
PrimaryReduction in Primary Joint Contracture to 5° or LessWithin 30 days after last injectionSuccessfully treated or clinical success in primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection.
SecondaryClinical Improvement in Primary Joint After the Last InjectionBaseline, Within 30 days after last injectionClinical improvement in primary joint defined as ≥50% reduction from baseline in the degree of contracture within 30 days after injection
SecondaryPercent Reduction From Baseline Contracture of Primary Joint After the Last InjectionBaseline, Day 30 after last injectionPercent change in degree of contracture of primary joint measured as 100 \* (baseline contracture - last available post-injection contracture)/baseline contracture
SecondaryChange From Baseline Range of Motion in Primary Joint After the Last InjectionBaseline, Day 30 after last injectionChange in degree of range of motion in primary joint measured as last available post-injection range of motion - baseline range of motion
SecondaryTime to Reach Clinical Success in Primary JointWithin 30 days after last injectionClinical success in primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection, displayed in post injection time point categories
SecondaryClinical Success in Primary Joint After the First InjectionWithin 30 days after first injectionClinical success in primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection.
SecondaryClinical Improvement in Primary Joint After the First InjectionBaseline, Within 30 days after first injectionClinical improvement in primary joint defined as ≥50% reduction from baseline in the degree of contracture within 30 days after injection
SecondaryPercent Reduction From Baseline Contracture of Primary Joint After the First InjectionBaseline, Day 30 after first injectionPercent change in degree of contracture of primary joint measured as 100 \* (baseline contracture - last available post-injection contracture prior to next injection)/baseline contracture
SecondaryChange From Baseline Range of Motion in Primary Joint After the First InjectionBaseline, Day 30 after first injectionChange in degree of range of motion in primary joint measured as last available post-injection range of motion prior to the next injection - baseline range of motion
SecondaryReduction in Non-primary Joint Contracture to 5° or Less After the Last InjectionWithin 30 days after last injectionSuccessfully treated or clinical success in non-primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection.
SecondaryClinical Improvement in Non-Primary Joint After the Last InjectionBaseline, Within 30 days after last injectionClinical improvement in non-primary joint defined as ≥50% reduction from baseline in the degree of contracture within 30 days after injection
SecondaryPercent Reduction From Baseline Contracture of Non-Primary Joint After the Last InjectionBaseline, Day 30 after last injectionPercent change in degree of contracture of non-primary joint measured as 100 \* (baseline contracture - last available post-injection contracture)/baseline contracture
SecondaryChange From Baseline Range of Motion in Non-Primary Joint After the Last InjectionBaseline, Day 30 after last injectionChange in degree of range of motion in non-primary joint measured as last available post-injection range of motion - baseline range of motion
SecondaryTime to Reach Clinical Success in Non-Primary JointWithin 30 days after last injectionClinical success in non-primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection, displayed in post injection time point categories
SecondaryClinical Success in Non-Primary Joint After the First InjectionWithin 30 days after first injectionClinical success in non-primary joint defined as reduction in contracture to within 0-5° of normal within 30 days of injection.
SecondaryClinical Improvement in Non-Primary Joint After the First InjectionBaseline, Within 30 days after first injectionClinical improvement in non-primary joint defined as ≥50% reduction from baseline in the degree of contracture within 30 days after injection
SecondaryPercent Reduction From Baseline Contracture of Non-Primary Joint After the First InjectionBaseline, Day 30 after first injectionPercent change in degree of contracture of non-primary joint measured as 100 \* (baseline contracture - last available post-injection contracture prior to next injection)/baseline contracture
SecondaryChange From Baseline Range of Motion in Non-Primary Joint After the First InjectionBaseline, Day 30 after first injectionChange in degree of range of motion in non-primary joint measured as last available post-injection range of motion prior to the next injection - baseline range of motion

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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