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Trial · NCT01483963

Outcomes13

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline to Day 92 in Active Forward FlexionBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Passive Forward FlexionBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Active AbductionBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Passive AbductionBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Active External RotationBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Passive External RotationBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Active Internal RotationBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in Passive Internal RotationBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
degreesMEAN
SECONDARYChange From Baseline to Day 92 in American Shoulder and Elbow Surgeons (ASES) Composite ScoreBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
units on a scaleMEAN
SECONDARYChange From Baseline to Day 92 in ASES Pain SubscaleBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
units on a scaleMEAN
SECONDARYChange From Baseline to Day 92 in ASES Function SubscaleBaseline, Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
units on a scaleMEAN
SECONDARYSubject Satisfaction With Treatment at Day 92Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYInvestigator Assessment of Improvement With Treatment at Day 92Day 92
All participants who have a baseline AROM measurement of the affected shoulder and at least 1 measurement of AROM of the affected shoulder following the first administration of study drug (AA4500 groups) or post baseline (shoulder exercises only group)
ParticipantsCOUNT_OF_PARTICIPANTS

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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