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Trial · NCT01494532

Results by group144

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group A: Placebo-1.9195% Confidence Interval -2.46 to -1.35Hours
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group B: 4 mg/Day-2.0495% Confidence Interval -3.02 to -1.06Hours
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group C: 8 mg/Day-2.9295% Confidence Interval -3.50 to -2.34Hours
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group D: 12 mg/Day-2.3495% Confidence Interval -2.91 to -1.76Hours
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group E: 16 mg/Day-2.8095% Confidence Interval -3.36 to -2.24Hours
Change From Baseline (BL) in Total Awake Time Spent Off at Week 4 of Maintenance PeriodTreatment Group F: 24 mg/Day-2.3795% Confidence Interval -3.26 to -1.47Hours
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group A: Placebo65.495% Confidence Interval 52.4 to 76.4percentage of participants
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group B: 4 mg/Day68.095% Confidence Interval 46.6 to 83.8percentage of participants
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group C: 8 mg/Day75.495% Confidence Interval 63.0 to 84.6percentage of participants
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group D: 12 mg/Day64.395% Confidence Interval 50.8 to 75.8percentage of participants
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group E: 16 mg/Day77.995% Confidence Interval 66.0 to 86.5percentage of participants
Responder Rate Defined as the Percentage of Participants With a 20% Reduction in Baseline (BL) Off Time at Week-4 of Maintenance PeriodTreatment Group F: 24 mg/Day72.095% Confidence Interval 51.1 to 86.4percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group A: Placebo72.195% Confidence Interval 59.5 to 82.0percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group B: 4 mg/Day70.195% Confidence Interval 48.6 to 85.4percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group C: 8 mg/Day80.695% Confidence Interval 68.7 to 88.7percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group D: 12 mg/Day73.595% Confidence Interval 59.6 to 83.9percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group E: 16 mg/Day83.295% Confidence Interval 72.1 to 90.5percentage of participants
Percentage of Participants With a >=1 Hour Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group F: 24 mg/Day81.495% Confidence Interval 62.3 to 92.0percentage of participants
Percentage of Participants With a >=2 Hours Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group A: Placebo53.795% Confidence Interval 39.8 to 67.1percentage of participants
Percentage of Participants With a >=2 Hours Reduction in Baseline Off Time at Week 4 of the Maintenance PeriodTreatment Group B: 4 mg/Day45.695% Confidence Interval 26.8 to 65.8percentage 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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