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Comparison · NCT06680206-e60d62c2

Rimegepant (Users With <12 Days of Use) vs Triptans: Number of Participants With Family Practitioner Visits in Past 6 Months- Sensitivity 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 (Users With <12 Days of Use) vs Triptans: Number of Participants With Family Practitioner Visits in Past 6 Months- Sensitivity Analysis. Trial comparisons, record NCT06680206-e60d62c2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT06680206-e60d62c2

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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 10.7380.6450.813wilson
Risk in group 20.7760.7530.799wilson
Risk difference, group 1 minus group 2-0.0386-0.1340.0404newcombe hybrid score
Risk ratio, group 1 over group 20.950.8441.07log
Odds ratio, group 1 over group 20.810.5121.28log
Number needed to treat, for one fewer participant with the outcome on Rimegepant (Users With <12 Days of Use) than on Triptans25.9from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Rimegepant (Users With <12 Days of Use)
Participants who were acute rimegepant users with days of use \< 12 days per month for migraine at the time of survey (NHWS in Year 2023) were included. No intervention was administered as a part of this study.
76103OG000
Group 2TriptansParticipants who responded to use triptans orally for migraine at the time of survey (NHWS in Year 2023) were included. No intervention was administered as a part of this study.9761,257OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Family Practitioner Visits in Past 6 Months- Sensitivity 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 months of this observational study.
Population
Analysis population included all eligible participants whose data were retrieved and observed in the study. For sensitivity analysis a subset of rimegepant users with less than 12 days of rimegepant use per month were included and the numbers were adjusted using IPTW method, which created pseudo population, leading to difference from the sample sizes before IPTW.

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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