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Comparison · NCT00000620-a998406a

Lipid Trial: Fenofibrate vs Lipid Trial: Placebo: First Occurrence of Major Cardiovascular Event (MCE) in the Lipid Trial.

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. Lipid Trial: Fenofibrate vs Lipid Trial: Placebo: First Occurrence of Major Cardiovascular Event (MCE) in the Lipid Trial. Trial comparisons, record NCT00000620-a998406a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00000620-a998406a

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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 10.1050.09430.117wilson
Risk in group 20.1130.1010.125wilson
Risk difference, group 1 minus group 2-0.00736-0.02380.0091newcombe hybrid score
Risk ratio, group 1 over group 20.9350.8041.09log
Odds ratio, group 1 over group 20.9270.7821.1log
Number needed to treat, for one fewer participant with the outcome on Lipid Trial: Fenofibrate than on Lipid Trial: Placebo136from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Lipid Trial: Fenofibrate
Double blind administration of 160 mg/day of fenofibrate in participants with estimated glomerular filtration rate (eGFR) ≥50 mL/min/1.73m\^2 or 54 mg/day in patients with eGFR \<50 mL/min/1.73m\^2, in combination with open label simvastatin 20 - 40 mg/day.
2912,765OG000
Group 2Lipid Trial: Placebo
Double blind administration of placebo matching either 160 mg/day in participants with eGFR ≥50 mL/min/1.73m\^2 or 54 mg/day in participants with eGFR \<50 mL/min/1.73m\^2, in combination with open label simvastatin 20 - 40 mg/day.
3102,753OG001

Outcome

Type
PRIMARY
Title
First Occurrence of Major Cardiovascular Event (MCE) in the Lipid Trial.
Description
Time to first occurrence of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death in Lipid Trial participants.
Time frame
4.7 years
Population
The population analyzed included all participants randomized and was performed by intention to treat with right-censoring of participants who did not complete follow-up prior to occurrence of MCE.

Source ClinicalTrials.gov

Trial

Title
Action to Control Cardiovascular Risk in Diabetes (ACCORD)
NCT number
NCT00000620
Phases
PHASE3
Conditions
Atherosclerosis, Cardiovascular Diseases, Hypercholesterolemia, Hypertension, Diabetes Mellitus, Type 2, Diabetes Mellitus, Coronary Disease
Interventions
Anti-hyperglycemic Agents, Anti-hypertensive Agents, Blinded fenofibrate or placebo plus simvastatin
Lead sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Results first posted
2014-09-15

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.govNone 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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