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Comparison · NCT00405275-sae

Triple vs Etanercept: 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. Triple vs Etanercept: serious adverse events. Trial comparisons, record NCT00405275-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00405275-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 10.1710.1270.226wilson
Risk in group 20.1960.1490.254wilson
Risk difference, group 1 minus group 2-0.0252-0.09760.0473newcombe hybrid score
Risk ratio, group 1 over group 20.8720.5881.29log
Odds ratio, group 1 over group 20.8450.5221.37log
Number needed to treat, for one fewer participant with a serious adverse event on Triple than on Etanercept39.7from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TripleHydroxychloroquine, sulfasalazine and methotrexate38222EG000
Group 2EtanerceptEtanercept and Methotrexate43219EG001

Harm

What it counts
Total, serious adverse events
Time frame
Beginning at Informed Consent until each participant's last study follow-up contact (expected to be 48 weeks), including a period of 30 days after last contact for SAE reporting.

Source ClinicalTrials.gov

Trial

Title
Rheumatoid Arthritis: Comparison of Active Therapies in Patients With Active Disease Despite Methotrexate Therapy
NCT number
NCT00405275
Phases
NA
Conditions
Rheumatoid Arthritis
Interventions
Etanercept, methotrexate, Sulfasalazine, Hydroxychloroquine, Placebo, triple, Placebo, etanercept
Lead sponsor
US Department of Veterans Affairs
Results first posted
2013-12-03

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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