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Trial · NCT01262677

Results by group414

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

OutcomeGroupCategoryValueSpreadUnits
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePregabalin 165 mgBaseline2.24Standard Deviation 0.757ln (seizures per 28 days)
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePregabalin 330 mgBaseline2.33Standard Deviation 0.873ln (seizures per 28 days)
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePlaceboBaseline2.32Standard Deviation 0.910ln (seizures per 28 days)
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePregabalin 165 mgWeek 141.84Standard Deviation 1.003ln (seizures per 28 days)
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePregabalin 330 mgWeek 141.80Standard Deviation 1.030ln (seizures per 28 days)
Log Transformed (Loge) 28-day Seizure Rate for All Partial Onset Seizures During the Double-blind Treatment PhasePlaceboWeek 141.93Standard Deviation 1.132ln (seizures per 28 days)
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePregabalin 165 mgResponder37.8percentage of participants
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePregabalin 330 mgResponder45.9percentage of participants
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePlaceboResponder35.8percentage of participants
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePregabalin 165 mgNon-responder62.2percentage of participants
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePregabalin 330 mgNon-responder54.1percentage of participants
Percentage of Participants With a ≥50% Reduction in the 28-day Partial Seizure Rate From Baseline During the Double-blind Treatment PhasePlaceboNon-responder64.2percentage of participants
Percentage Change From Baseline in 28-day Partial Seizure Rate During the Double-blind Treatment PhasePregabalin 165 mg-15.00Standard Error 11.668ln (seizures per 28 days)
Percentage Change From Baseline in 28-day Partial Seizure Rate During the Double-blind Treatment PhasePregabalin 330 mg-31.54Standard Error 10.772ln (seizures per 28 days)
Percentage Change From Baseline in 28-day Partial Seizure Rate During the Double-blind Treatment PhasePlacebo-5.70Standard Error 10.918ln (seizures per 28 days)
Frequency of Secondary Generalized Tonic-clonic Seizures (SGTC) During the Double-blind Treatment PhasePregabalin 165 mg3.99Standard Deviation 8.667seizures per 28 days
Frequency of Secondary Generalized Tonic-clonic Seizures (SGTC) During the Double-blind Treatment PhasePregabalin 330 mg4.43Standard Deviation 14.736seizures per 28 days
Frequency of Secondary Generalized Tonic-clonic Seizures (SGTC) During the Double-blind Treatment PhasePlacebo7.51Standard Deviation 24.979seizures per 28 days
Log Transformed 28-day SGTC Rate for All SGTCs During the Double-blind Maintenance PhasePregabalin 165 mg0.46Standard Error 0.049ln (seizures per 28 days)
Log Transformed 28-day SGTC Rate for All SGTCs During the Double-blind Maintenance PhasePregabalin 330 mg0.48Standard Error 0.045ln (seizures per 28 days)

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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