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Comparison · NCT00407745-2131a56c

Pregabalin vs Placebo: Number of Participants With Improved Duration of Brief Pain Attacks Based on NPSI - Duration (Item 4)

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: Number of Participants With Improved Duration of Brief Pain Attacks Based on NPSI - Duration (Item 4). Trial comparisons, record NCT00407745-2131a56c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00407745-2131a56c

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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 10.390.30.488wilson
Risk in group 20.2890.2080.386wilson
Risk difference, group 1 minus group 20.101-0.03080.228newcombe hybrid score
Risk ratio, group 1 over group 21.350.9082.01log
Odds ratio, group 1 over group 21.580.8692.86log
Number needed to treat, for one more participant with the outcome on Pregabalin than on Placebo9.87from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Pregabalin
Pregabalin 75 milligram (mg) capsule administered by mouth (PO) twice daily (BID) for 7 days. On Day 8, dose may have been maintained at 150 mg per day or increased to 300 mg per day. Each week thereafter, including at Visit 4, a dose increase or decrease may have occurred depending on clinical judgement on adequate pain relief and tolerability. Following the end of adjustment phase, at Visit 4, participants were at their optimized dose (150 mg per day, 300 mg per day, 450 mg per day, or 600 mg per day). Participants remained at this maintenance dose throughout the next 12 weeks of the study.
39100OG000
Group 2PlaceboPlacebo matching study treatment.2897OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Improved Duration of Brief Pain Attacks Based on NPSI - Duration (Item 4)
Description
NPSI - Temporal item which assesses the duration (number of hours during the last 24 hours) of spontaneous ongoing pain. Improved duration would be a decrease in the number of hours of spontaneous ongoing pain during the last 24 hours compared to baseline.
Time frame
Baseline, Week 16
Population
MITT; LOCF; (N) = number of participants with data available for analysis

Source ClinicalTrials.gov

Trial

Title
A 17-Week Trial To Assess Pregabalin For The Treatment Of Nerve Pain Due To Spinal Cord Injury
NCT number
NCT00407745
Phases
PHASE3
Conditions
Neuralgia, Spinal Cord Injuries
Interventions
placebo, pregabalin
Lead sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
Results first posted
2011-12-08

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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