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Trial · NCT06065670

Registered outcomes48

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryCorpus Callosum Myelin Water FractionThis will be assessed at the baseline visit.The efficacy of clemastine relative to placebo at increasing the myelin water fraction (MWF) (measured in %) from magnetic resonance imaging of the corpus callosum.
PrimaryChange from Baseline in Corpus Callosum Myelin Water Fraction at 3 MonthsThis will be assessed at the baseline and 3 month visits.The efficacy of clemastine relative to placebo at increasing the myelin water fraction (MWF) (measured in %) from magnetic resonance imaging of the corpus callosum. Change = (3-month % - Baseline %)
PrimaryChange from Baseline in Corpus Callosum Myelin Water Fraction at 6 MonthsThis will be assessed at the baseline and 6 month visits.The efficacy of clemastine relative to placebo at increasing the myelin water fraction (MWF) (measured in %) from magnetic resonance imaging of the corpus callosum. Change = (6-month % - Baseline %)
PrimaryCorpus Callosum T1 Relaxation TimeThis will be assessed at the baseline visit.The efficacy of clemastine relative to placebo at shortening the T1 relaxation time (measured in seconds) within the corpus callosum using T1 mapping protocols in an MRI.
PrimaryChange from Baseline in Corpus Callosum T1 Relaxation Time at 3 MonthsThis will be assessed at the baseline and 3-month visits.
The efficacy of clemastine relative to placebo at shortening the T1 relaxation time (measured in seconds) within the corpus callosum using T1 mapping protocols in an MRI. (3-month time - Baseline time)
PrimaryChange from Baseline in Corpus Callosum T1 Relaxation Time at 6 MonthsThis will be assessed at the baseline and 6-month visits.
The efficacy of clemastine relative to placebo at shortening the T1 relaxation time (measured in seconds) within the corpus callosum using T1 mapping protocols in an MRI. (6-month time - Baseline time)
PrimaryCorpus Callosum UTE FractionThis will be assessed at the baseline visit.The efficacy of clemastine relative to placebo at increasing the ultrashort echo time (UTE) fraction (measured in %) derived from magnetic resonance imaging of the corpus callosum.
PrimaryChange from Baseline in Corpus Callosum UTE Fraction at 3 MonthsThis will be assessed at the baseline and 3-month visits.
The efficacy of clemastine relative to placebo at increasing the ultrashort echo time (UTE) fraction (measured in %) derived from magnetic resonance imaging of the corpus callosum. Change = (3-month % - Baseline %)
PrimaryChange from Baseline in Corpus Callosum UTE Fraction at 6 MonthsThis will be assessed at the baseline and 6-month visits.
The efficacy of clemastine relative to placebo at increasing the ultrashort echo time (UTE) fraction (measured in %) derived from magnetic resonance imaging of the corpus callosum. Change = (6-month % - Baseline %)
SecondaryOptic Radiation Myelin Water FractionThis will be assessed at the baseline visit.The efficacy of Clemastine relative to placebo at increasing the MWF (measured in %) of the optic radiation.
SecondaryChange from Baseline in Optic Radiation Myelin Water Fraction at 3 MonthsThis will be assessed at the baseline and 3-month visits.The efficacy of Clemastine relative to placebo at increasing the MWF (measured in %) of the optic radiation. Change = (3-month % - Baseline %)
SecondaryChange from Baseline in Optic Radiation Myelin Water Fraction at 6 MonthsThis will be assessed at the baseline and 6-month visits.The efficacy of Clemastine relative to placebo at increasing the MWF (measured in %) of the optic radiation. Change = (6-month % - Baseline %)
SecondaryCorticospinal Tract Myelin Water FractionThis will be assessed at the baseline visit.The efficacy of clemastine relative to placebo at increasing the MWF (measured in %) of the corticospinal tract.
SecondaryChange from Baseline in Corticospinal Tract Myelin Water Fraction at 3 MonthsThis will be assessed at the baseline and 3-month visits.The efficacy of clemastine relative to placebo at increasing the MWF (measured in %) of the corticospinal tract. (3-month % - Baseline %)
SecondaryChange from Baseline in Corticospinal Tract Myelin Water Fraction at 6 MonthsThis will be assessed at the baseline and 6-month visits.The efficacy of clemastine relative to placebo at increasing the MWF (measured in %) of the corticospinal tract. (6-month % - Baseline %)
SecondaryOptic Radiation T1 Relaxation timeThis will be assessed at the baseline visit.To evaluate the efficacy of Clemastine relative to placebo at increasing the T1 relaxation time (measured in seconds) of the optic radiation.
SecondaryChange from Baseline in Optic Radiation T1 Relaxation time at 3 MonthsThis will be assessed at the baseline and 3-month visits.To evaluate the efficacy of Clemastine relative to placebo at increasing the T1 relaxation time (measured in seconds) of the optic radiation. (3-month time - Baseline time)
SecondaryChange from Baseline in Optic Radiation T1 Relaxation time at 6 MonthsThis will be assessed at the baseline and 6-month visits.To evaluate the efficacy of Clemastine relative to placebo at increasing the T1 relaxation time (measured in seconds) of the optic radiation. (6-month time - Baseline time)
SecondaryCorticospinal Tract T1 Relaxation TimeThis will be assessed at the baseline visit.To evaluate the efficacy of Clemastine relative to placebo at increasing the T1 relaxation time (measured in seconds) of the corticospinal tract.
SecondaryChange from Baseline in Corticospinal Tract T1 Relaxation Time at 3 MonthsThis will be assessed at the baseline and 3-month visits.To evaluate the efficacy of Clemastine relative to placebo at increasing the T1 relaxation time (measured in seconds) of the corticospinal tract. (3-month time - Baseline time)

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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