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Comparison · NCT00567268-2d560bc4

Presence of Non-Drug Therapy vs Absence of Non-Drug Therapy: Number of Participants Who Responded to Treatment With Gabapentin by Presence or Absence of Non-Drug Therapy

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. Presence of Non-Drug Therapy vs Absence of Non-Drug Therapy: Number of Participants Who Responded to Treatment With Gabapentin by Presence or Absence of Non-Drug Therapy. Trial comparisons, record NCT00567268-2d560bc4. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00567268-2d560bc4

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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 10.7560.6130.858wilson
Risk in group 20.6050.5740.635wilson
Risk difference, group 1 minus group 20.1510.005170.257newcombe hybrid score
Risk ratio, group 1 over group 21.251.051.49log
Odds ratio, group 1 over group 22.021.014.03log
Number needed to treat, for one more participant with the outcome on Presence of Non-Drug Therapy than on Absence of Non-Drug Therapy6.643.89193from 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 1Presence of Non-Drug TherapyParticipants with non-drug therapy who responded to treatment with gabapentin3445OG000
Group 2Absence of Non-Drug TherapyParticipants without non-drug therapy who responded to treatment with gabapentin6051,000OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Participants Who Responded to Treatment With Gabapentin by Presence or Absence of Non-Drug Therapy
Description
Participants who responded to the treatment with gabapentin were counted by the presence or absence of non-drug therapy to assess whether the non-drug therapy was a factor affecting the treatment efficacy.
Time frame
12 weeks
Population
The efficacy analysis population comprised of the participants who had at least one post-baseline efficacy evaluation for the clinical efficacy and seizure frequency in the safety analysis population. Participants who had diseases not eligible for the survey were excluded from the efficacy analysis population.

Source ClinicalTrials.gov

Trial

Title
Drug Use Investigation Of Gabapentin
NCT number
NCT00567268
Phases
Conditions
Epilepsies, Partial
Interventions
Gabapentin
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Results first posted
2015-05-12

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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