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Comparison · NCT06680206-df774e3d

Rimegepant vs Triptans: Number of Participants With Neurologist Visits in Past 6 Months - Primary Analysis

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Rimegepant vs Triptans: Number of Participants With Neurologist Visits in Past 6 Months - Primary Analysis. Trial comparisons, record NCT06680206-df774e3d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT06680206-df774e3d

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.5330.4490.615wilson
Risk in group 20.2970.2720.323wilson
Risk difference, group 1 minus group 20.2370.1490.322newcombe hybrid score
Risk ratio, group 1 over group 21.81.52.15log
Odds ratio, group 1 over group 22.711.893.88log
Number needed to treat, for one more participant with the outcome on Rimegepant than on Triptans4.233.16.72from the risk difference interval

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1RimegepantParticipants with self-reported diagnosis of migraine currently on rimegepant use at the time of survey (NHWS in year 2023) were included. No intervention was administered as part of this study.72135OG000
Group 2TriptansParticipants with self-reported diagnosis of migraine currently on triptan use at the time of survey (NHWS in year 2023) were included. No intervention was administered as part of this study.3741,260OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Neurologist Visits in Past 6 Months - Primary Analysis
Description
Analysis was performed using IPTW method to adjust for confounding by the covariates.
Time frame
6 months before the survey was taken, during 1 year of data identification (Year 2023); available retrospective data was evaluated over approximately 1.41 month of this observational study.
Population
Analysis population included all eligible participants whose data were retrieved and observed in the study and were adjusted using IPTW method (pseudo-set); hence, numbers of participants are different here from those presented in participant flow and baseline section.

Source ClinicalTrials.gov

Trial

Title
Comparison of Patient-reported Outcomes for Rimegepant and Triptans in the 2023 US National Health and Wellness Survey
NCT number
NCT06680206
Phases
Conditions
Migraine
Interventions
Rimegepant, Triptans
Lead sponsor
Pfizer
Results first posted
2026-01-22

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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