ConductScience.org, home

Library / Trial comparisons

Novasoy vs Placebo: Number of Participants With ApoE4 Allele

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 10.50.3360.664wilsonClinicalTrials.gov
Risk in group 20.4550.2980.62wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.0455-0.1870.272newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.10.6611.83logClinicalTrials.gov
Odds ratio, group 1 over group 21.20.4533.18logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Novasoy than on Placebo22from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Novasoy100mg/day soy isoflavones~Novasoy: 100mg/day soy isoflavones1632OG001ClinicalTrials.gov
Group 2Placebo100mg/day matching placebo~Placebo: 100mg/day matching placebo1533OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With ApoE4 AlleleClinicalTrials.gov
Description
The epsilon-4 allele of the apolipoprotein E gene (APOE4) has been consistently associated with a greater risk of Alzheimer's disease (AD) as well as an earlier onset of AD.~Determination of apolipoprotein E (APOE) genotype was performed on a non-fasting blood sample collected at Baseline, using standard Polymerase chain reaction (PCR) and DNA sequencing techniques in a Clinical Laboratory Improvement Amendments (CLIA) certified laboratory. DNA extracted from whole blood was amplified by PCR using specific primers for the ApoE gene and the DNA then sequenced and analyzed for genotype using the FinchTV program (Version 1.3; Geospiza, Inc.)
ClinicalTrials.gov
Time frameBaselineClinicalTrials.gov
PopulationOlder adults with Alzheimer's diseaseClinicalTrials.gov

Trial 8

FieldValueSource
TitleAlzheimer's Disease: Potential Benefit of IsoflavonesClinicalTrials.gov
NCT numberNCT00205179ClinicalTrials.gov
PhasesPHASE2ClinicalTrials.gov
ConditionsAlzheimer's DiseaseClinicalTrials.gov
InterventionsNovasoy, PlaceboClinicalTrials.gov
Lead sponsorUniversity of Wisconsin, MadisonClinicalTrials.gov
Results first posted2020-01-22ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT00205179?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.