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Comparison · NCT01080300-sae

G-ER 1800 mg vs Sugar Pill: 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. G-ER 1800 mg vs Sugar Pill: serious adverse events. Trial comparisons, record NCT01080300-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01080300-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 10.01330.00520.0338wilson
Risk in group 20.02370.01150.0482wilson
Risk difference, group 1 minus group 2-0.0104-0.03610.0134newcombe hybrid score
Risk ratio, group 1 over group 20.5620.1661.9log
Odds ratio, group 1 over group 20.5560.1611.92log
Number needed to treat, for one fewer participant with a serious adverse event on G-ER 1800 mg than on Sugar Pill96.2from 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 1G-ER 1800 mgGabapentin extended-release (G-ER) 1800 mg4300EG000
Group 2Sugar PillPlacebo 1800 mg7295EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events collected for a total of 28-42 weeks: from after signing the informed consent to the end of the study (Week 28).

Source ClinicalTrials.gov

Trial

Title
Breeze3:Study of Gabapentin Extended Release in the Treatment of Vasomotor Symptoms(Hot Flashes)in Postmenopausal Women
NCT number
NCT01080300
Phases
PHASE3
Conditions
Hot Flashes
Interventions
Gabapentin Extended Release, Placebo
Lead sponsor
Depomed
Results first posted
2014-03-26

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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