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Comparison · NCT00432744-sae

CoenzymeQ10 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. CoenzymeQ10 vs Placebo: serious adverse events. Trial comparisons, record NCT00432744-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00432744-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 10.05260.009350.246wilson
Risk in group 20.10.02790.301wilson
Risk difference, group 1 minus group 2-0.0474-0.2530.159newcombe hybrid score
Risk ratio, group 1 over group 20.5260.05195.34log
Odds ratio, group 1 over group 20.50.04156.02log
Number needed to treat, for one fewer participant with a serious adverse event on CoenzymeQ10 than on Placebo21.1from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1CoenzymeQ10CoenzymeQ10: CoenzymeQ10 will be given in 10 mg/kg daily up to 400 mg. Then a draw of CoQ10 troughs every three months will be performed. (Either in Period 1 or Period 2)119EG000
Group 2Placebo
Placebo: Placebo will be given in 10 mg/kg daily up to 400 mg. Then a draw of placebo troughs every three months will be performed. This treatment group will be treated as the active group. (Either in Period 1 or Period 2)
220EG001

Harm

What it counts
Total, serious adverse events
Time frame
AE's were collected from 10/2007 to 4/2012.

Source ClinicalTrials.gov

Trial

Title
Phase III Trial of Coenzyme Q10 in Mitochondrial Disease
NCT number
NCT00432744
Phases
PHASE3
Conditions
Mitochondrial Diseases
Interventions
CoenzymeQ10, Placebo
Lead sponsor
University of Florida
Results first posted
2014-05-01

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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