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Trial · NCT03103919

Outcomes15

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYChange From Baseline to Visit 2 in Unified Parkinson's Disease Rating Scale (UPDRS) Part III Motor ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12/ 3 months after start of treatment with Neupro)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Finger Tapping Speed ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Rest Tremor ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Averaged Finger Tapping Speed and Resting Tremor ScoresBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Postural Tremor ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Finger Tapping Amplitude ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Hand Grasp Speed ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Hand Grasp Amplitude ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Rapid Alternating Movement Speed ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Rapid Alternating Amplitude ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYChange From Baseline to Visit 2 in Kinesia-ONE™ Variable: Dyskinesia ScoreBaseline (Visit 1/Week 1) to Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.Scores on a scaleLEAST_SQUARES_MEAN
PRIMARYNeupro Dose Per 24h at Visit 2 (Week 12)Visit 2 (Week 12)The Full Analysis Set (FAS) included all subjects who had at least 1 valid Baseline and at least 1 valid post-Baseline efficacy measurement.mg/24 hrMEAN
PRIMARYNumber of Neupro Dose Changes During the StudyVisit 1 (Week 1) to Visit 2 (Week 12)The Safety Set (SS) included all subjects who received at least 1 dose of Neupro.dose changesMEAN
PRIMARYNumber of Subjects Who Discontinued the Treatment With Neupro During the Course of the StudyVisit 1 (Week 1) to Visit 2 (Week 12)The Safety Set (SS) included all subjects who received at least 1 dose of Neupro.ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYNumber of Subjects With Any Adverse Events During the Course of the StudyVisit 1 (Week 1) to Visit 2 (Week 12)The Safety Set (SS) included all subjects who received at least 1 dose of Neupro.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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT03103919/outcomes