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Trial · NCT01154166

Results by group40

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Mean Change From Baseline in Total Awake Time Spent Off at Week 24 Using Last Observation Carried Forward (LOCF)Placebo-0.4Standard Deviation 2.47hours
Mean Change From Baseline in Total Awake Time Spent Off at Week 24 Using Last Observation Carried Forward (LOCF)Ropinirole PR-2.1Standard Deviation 2.58hours
Mean Change From Baseline (BL) in the Unified Parkinson Disease Rating Scale (UPDRS) Total Motor Score at Week 24 Using LOCFPlacebo-0.7Standard Deviation 9.03scores on a scale
Mean Change From Baseline (BL) in the Unified Parkinson Disease Rating Scale (UPDRS) Total Motor Score at Week 24 Using LOCFRopinirole PR-6.3Standard Deviation 10.08scores on a scale
Mean Change From Baseline in the Percentage of Awake Time Spent Off (ATSO) at Week 24 Using LOCFPlacebo-1.8Standard Deviation 15.88Percentage of time
Mean Change From Baseline in the Percentage of Awake Time Spent Off (ATSO) at Week 24 Using LOCFRopinirole PR-13.5Standard Deviation 15.62Percentage of time
Mean Change From Baseline in Total Awake Time Spent on at Week 24 Using LOCFPlacebo0.1Standard Deviation 2.48hours
Mean Change From Baseline in Total Awake Time Spent on at Week 24 Using LOCFRopinirole PR1.9Standard Deviation 2.44hours
Mean Change From Baseline in Total Awake Time on Without Troublesome Dyskinesias (TD) at Week 24 Using LOCFPlacebo0.3Standard Deviation 2.56hours
Mean Change From Baseline in Total Awake Time on Without Troublesome Dyskinesias (TD) at Week 24 Using LOCFRopinirole PR1.7Standard Deviation 2.81hours
Mean Change From Baseline in the UPDRS Activities of Daily Living (ADL) Score at Week 24 Using LOCFPlacebo-0.2Standard Deviation 3.64scores on a scale
Mean Change From Baseline in the UPDRS Activities of Daily Living (ADL) Score at Week 24 Using LOCFRopinirole PR-2.2Standard Deviation 3.93scores on a scale
Number of Responders Based on the Clinical Global Impression (CGI) Global Improvement Scale Using LOCFPlacebo16participants
Number of Responders Based on the Clinical Global Impression (CGI) Global Improvement Scale Using LOCFRopinirole PR77participants
Number of Participants Requiring Reinstatement of L-dopa Following a Dose Reduction Using LOCFPlacebo23participants
Number of Participants Requiring Reinstatement of L-dopa Following a Dose Reduction Using LOCFRopinirole PR13participants
Number of Responders to Study Treatment Using LOCFPlacebo4participants
Number of Responders to Study Treatment Using LOCFRopinirole PR39participants
Mean Change From Baseline in the Depression Scores on the Hamilton Depression Rating Scale (HAMD-17) Using LOCFPlacebo-0.6Standard Deviation 4.33scores on a scale
Mean Change From Baseline in the Depression Scores on the Hamilton Depression Rating Scale (HAMD-17) Using LOCFRopinirole PR-1.6Standard Deviation 4.38scores on a scale

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/NCT01154166/results