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Comparison · NCT01117181-sae

Methylphenidate 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. Methylphenidate vs Placebo: serious adverse events. Trial comparisons, record NCT01117181-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01117181-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 10.03450.006110.172wilson
Risk in group 20.03230.005720.162wilson
Risk difference, group 1 minus group 20.00222-0.1310.142newcombe hybrid score
Risk ratio, group 1 over group 21.070.070116.3log
Odds ratio, group 1 over group 21.070.063918log
Number needed to harm, for one more participant with a serious adverse event on Methylphenidate than on Placebo449from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MethylphenidateMethylphenidate, target dose 20 mg per day (range 10-20 mg per day) and psychosocial intervention129EG000
Group 2Placebomatching placebo and psychosocial intervention131EG001

Harm

What it counts
Total, serious adverse events
Time frame
treatment period (i.e., 6 weeks)

Source ClinicalTrials.gov

Trial

Title
Apathy in Dementia Methylphenidate Trial (ADMET)
NCT number
NCT01117181
Phases
PHASE2
Conditions
Apathy, Alzheimer's Disease
Interventions
Methylphenidate, placebo, Psychosocial intervention
Lead sponsor
Johns Hopkins Bloomberg School of Public Health
Results first posted
2013-05-10

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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