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Trial · NCT03467152

Results by group130

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

OutcomeGroupCategoryValueSpreadUnits
Change From Baseline in the Montreal Cognitive Assessment (MoCA) Total Score at Week 12 of TreatmentPlaceboBaseline13.9Standard Deviation 5.40score on a scale
Change From Baseline in the Montreal Cognitive Assessment (MoCA) Total Score at Week 12 of TreatmentIrsenontrine 50 mgBaseline13.8Standard Deviation 5.18score on a scale
Change From Baseline in the Montreal Cognitive Assessment (MoCA) Total Score at Week 12 of TreatmentPlaceboChange at Week 12-0.6Standard Deviation 2.63score on a scale
Change From Baseline in the Montreal Cognitive Assessment (MoCA) Total Score at Week 12 of TreatmentIrsenontrine 50 mgChange at Week 12-0.4Standard Deviation 3.41score on a scale
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboMarked improvement0Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgMarked improvement0Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboModerate improvement5Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgModerate improvement3Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboMinimal improvement13Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgMinimal improvement18Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboNo change32Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgNo change32Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboMinimal worsening30Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgMinimal worsening28Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboModerate worsening6Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgModerate worsening8Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentPlaceboMarked worsening0Participants
Number of Participants Based on Clinician's Interview Based Impression of Change Plus Caregiver Input (CIBIC-Plus) Scale at Week 12 of TreatmentIrsenontrine 50 mgMarked worsening0Participants
Clinician's Global Impression of Change - In Dementia With Lewy Bodies (CGIC-DLB) Scale at Week 12 of TreatmentPlaceboMarked improvement1Participants
Clinician's Global Impression of Change - In Dementia With Lewy Bodies (CGIC-DLB) Scale at Week 12 of TreatmentIrsenontrine 50 mgMarked improvement0Participants

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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