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Comparison · NCT00469456-sae

Memantine 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. Memantine vs Placebo: serious adverse events. Trial comparisons, record NCT00469456-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00469456-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 10.02960.01160.0737wilson
Risk in group 20.1010.05980.165wilson
Risk difference, group 1 minus group 2-0.0711-0.138-0.011newcombe hybrid score
Risk ratio, group 1 over group 20.2940.09840.878log
Odds ratio, group 1 over group 20.2720.08640.859log
Number needed to treat, for one fewer participant with a serious adverse event on Memantine than on Placebo14.17.2691from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MemantineMemantine 20mg (10mg twice daily), oral administration for 12 weeks4135EG001
Group 2PlaceboMatching placebo, oral administration, twice daily for 12 weeks13129EG000

Harm

What it counts
Total, serious adverse events
Time frame
Occurring on or after the date of the first dose of double-blind study medication and within 30 days of the date of last dose of double-blind study medication.

Source ClinicalTrials.gov

Trial

Title
Effect of Memantine on Functional Communication in Patients With Alzheimer's Disease
NCT number
NCT00469456
Phases
PHASE4
Conditions
Alzheimer's Disease
Interventions
Memantine, placebo
Lead sponsor
Forest Laboratories
Results first posted
2009-12-07

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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