ConductScience.org, home

Trial · NCT06992674

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryModerate/Severe vestibular symptom daysfrom baseline to weeks 12-16Change in number of Moderate/Severe vestibular symptom days as defined by Barany Society1 for participants measured daily from the observational phase compared to weeks 12-16.
SecondaryModerate/Severe vestibular symptom daysevery 4 weeks during the 12-week treatment period compared to baselineChange in number of Moderate/Severe vestibular symptom days as defined by Barany Society1 every 4 weeks during the 12-week treatment period compared to baseline
Secondarythe number of vestibular symptom attacksevery 4 weeks compared to baseline over the 12-week treatment period
Change in the number of vestibular symptom attacks every 4 weeks compared to baseline over the 12-week treatment period. (Since VM attacks may recur multiple times within a day, each lasting a short duration, we need to further clearly define what constitutes "one attack.")
SecondaryMMDevery 4 weeks compared to baseline over the 12-week treatment periodChange in the number of monthly migraine days (MMD) every 4 weeks compared to baseline over the 12-week treatment period
SecondaryMIDASfrom baseline to week 16Change in Migraine Disability Assessment (MIDAS) score from baseline to week 16
Secondarypercentage reduction in moderate/severe vestibular symptom daysfrom baseline to weeks 12-16Change in response rate (100%,75%,50%,25%,0%) by percentage reduction in moderate/severe vestibular symptom days from baseline to weeks 12-16
SecondaryDHIfrom baseline to week 16Change in dizziness handicap inventory (DHI) score from baseline to week 16
SecondaryVADLfrom baseline to week 16Change in Vestibular Activities of Daily Living Scale (VADL) score from baseline to week 16
SecondaryPHQ-9from baseline to week 16Change in Patient Health Questionnaire-9 (PHQ-9) score from baseline to week 16
SecondaryGAD-7from baseline to week 16Change in General Anxiety Disorder-7 (GAD-7) score from baseline to week 16
SecondaryPGICfrom baseline to week 16Change in Patient Global Impression of Change(PGIC scale)from baseline to week 16
SecondaryMSQfrom baseline to week 16Change in Migraine-Specific Quality of Life (MSQ) score from baseline to week 16

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

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT06992674/registered