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Trial · NCT02019667

Results by group20

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline on the Adaptive Behavior Assessment System (ABAS) Test at the End of the Study Drug and Placebo Treatment PeriodsPlacebo5.2Standard Deviation 7.1scores on a scale
Change From Baseline on the Adaptive Behavior Assessment System (ABAS) Test at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug4.5Standard Deviation 7.5scores on a scale
Change From Baseline of TMS Measurement of Motor Threshold at the End of the Study Drug and Placebo Treatment PeriodsPlacebo-2Standard Deviation 7.1percentage of stimulator output
Change From Baseline of TMS Measurement of Motor Threshold at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug-0.5Standard Deviation 6.8percentage of stimulator output
Change From Baseline of TMS Measurement of Intracortical Facilitation at the End of the Study Drug and Placebo Treatment PeriodsPlacebo49.9Standard Deviation 61.9ratio of MEP amplitude
Change From Baseline of TMS Measurement of Intracortical Facilitation at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug40.5Standard Deviation 50.2ratio of MEP amplitude
Change From Baseline of TMS Measurement of Short Interval Intracortical Inhibition (Short ICI) at the End of the Study Drug and Placebo Treatment PeriodsPlacebo35.5Standard Deviation 123.4ratio of MEP amplitude
Change From Baseline of TMS Measurement of Short Interval Intracortical Inhibition (Short ICI) at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug-11.0Standard Deviation 54.8ratio of MEP amplitude
Change From Baseline of TMS Measurement of Long Interval Intracortical Inhibition (Long ICI) at the End of the Study Drug and Placebo Treatment PeriodsPlacebo-9.3Standard Deviation 112.0ratio of MEP amplitude
Change From Baseline of TMS Measurement of Long Interval Intracortical Inhibition (Long ICI) at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug0.3Standard Deviation 98.6ratio of MEP amplitude
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsPlacebo00Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug00Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsPlacebo114Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug115Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsPlacebo24Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug23Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsPlacebo30Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug30Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsPlacebo40Participants
Results of Physical Examination at the End of the Study Drug and Placebo Treatment PeriodsStudy Drug40Participants

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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