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Citicoline vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

Measures 6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.03130.005540.157wilsonClinicalTrials.gov
Risk in group 20.1430.0570.315wilsonClinicalTrials.gov
Risk difference, group 1 minus group 2-0.112-0.2860.041newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 20.2190.02591.84logClinicalTrials.gov
Odds ratio, group 1 over group 20.1940.02031.85logClinicalTrials.gov
Number needed to treat, for one fewer participant with a serious adverse event on Citicoline than on Placebo8.96from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1CiticolineCiticoline is an over the counter supplement that may have neuroprotective properties and may have antidepressant effects.132EG000ClinicalTrials.gov
Group 2Placebo428EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, serious adverse eventsClinicalTrials.gov
Time frameClinicalTrials.gov

Trial 8

FieldValueSource
TitleA Pilot Study of Citicoline add-on Therapy in Patients With Bipolar Disorder or Major Depressive Disorder and Amphetamine Abuse or DependenceClinicalTrials.gov
NCT numberNCT00377299ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsAmphetamine Abuse, Amphetamine Dependence, Bipolar Disorder, Major Depressive DisorderClinicalTrials.gov
InterventionsCiticoline, PlaceboClinicalTrials.gov
Lead sponsorUniversity of Texas Southwestern Medical CenterClinicalTrials.gov
Results first posted2013-08-08ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00377299?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.