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Comparison · NCT02394951-sae

Pregabalin vs Placebo: serious adverse events

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. Pregabalin vs Placebo: serious adverse events. Trial comparisons, record NCT02394951-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02394951-sae

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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 10.040.00710.195wilson
Risk in group 200.00000000000000001390.133wilson
Risk difference, group 1 minus group 20.04-0.09720.195newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more participant with a serious adverse event on Pregabalin than on Placebo25from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1PregabalinPregabalin administered for 4 weeks, titrated to highest tolerated dose up to 600 mg/day.~Pregabalin: Anticonvulsant~Placebo: Identical, matching inactive substance125EG000
Group 2PlaceboIdentical, matching inactive substance administered for 4 weeks following the same dosing regimen.~Pregabalin: Anticonvulsant~Placebo: Identical, matching inactive substance025EG001

Harm

What it counts
Total, serious adverse events
Time frame
11 weeks

Source ClinicalTrials.gov

Trial

Title
Pregabalin in CIPN
NCT number
NCT02394951
Phases
NA
Conditions
Neuropathy, Pain
Interventions
Pregabalin, Placebo
Lead sponsor
Washington University School of Medicine
Results first posted
2019-05-14

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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