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Comparison · NCT01940523-32a5cd36

IV TXA Group vs Topical TXA Group: The Number Patients Requiring a Transfusion

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. IV TXA Group vs Topical TXA Group: The Number Patients Requiring a Transfusion. Trial comparisons, record NCT01940523-32a5cd36. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01940523-32a5cd36

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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 10.006250.001720.0225wilson
Risk in group 20.01880.008620.0403wilson
Risk difference, group 1 minus group 2-0.0125-0.03450.00665newcombe hybrid score
Risk ratio, group 1 over group 20.3330.06781.64log
Odds ratio, group 1 over group 20.3290.06591.64log
Number needed to treat, for one fewer participant with the outcome on IV TXA Group than on Topical TXA Group80from 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 1IV TXA GroupKaitlin - Explain this group....2320OG000
Group 2Topical TXA GroupKaitlin - Explain this group6320OG001

Outcome

Type
SECONDARY
Title
The Number Patients Requiring a Transfusion
Description
TThe number Patients requiring a transfusion over the course of the patient's hospital stay.
Time frame
over course of hospital stay (averaging three days)
Population

Source ClinicalTrials.gov

Trial

Title
Randomized Controlled Trial of Tranexamic Acid in Total Knee Arthroplasty: Intravenous vs. Topical
NCT number
NCT01940523
Phases
PHASE4
Conditions
Osteoarthritis
Interventions
Topical Tranexamic Acid, Intravenous Tranexamic Acid
Lead sponsor
Hospital for Special Surgery, New York
Results first posted
2017-06-14

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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