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Comparison · NCT00119106-sae

Tenofovir 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. Tenofovir vs Placebo: serious adverse events. Trial comparisons, record NCT00119106-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00119106-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 10.1890.1670.212wilson
Risk in group 20.2030.1820.227wilson
Risk difference, group 1 minus group 2-0.0149-0.04660.0168newcombe hybrid score
Risk ratio, group 1 over group 20.9270.7881.09log
Odds ratio, group 1 over group 20.910.7441.11log
Number needed to treat, for one fewer participant with a serious adverse event on Tenofovir than on Placebo67from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TenofovirTenofovir~Tenofovir2271,204EG000
Group 2PlaceboPlacebo~Tenofovir2461,209EG001

Harm

What it counts
Total, serious adverse events
Time frame
Participants were assessed for adverse events from the date the participant enrolled and started study drug until the participant completed follow-up, a maximum of 6.9 years.

Source ClinicalTrials.gov

Trial

Title
Bangkok Tenofovir Study, an HIV Pre-exposure Prophylaxis Trial, Bangkok, Thailand
NCT number
NCT00119106
Phases
PHASE2, PHASE3
Conditions
HIV Infections
Interventions
Tenofovir disoproxil, Placebo
Lead sponsor
Centers for Disease Control and Prevention
Results first posted
2021-01-27

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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