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Comparison · NCT00032591-sae

Patient Self-Testing (PST) vs High Quality Anticoagulation Management (HQACM): 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. Patient Self-Testing (PST) vs High Quality Anticoagulation Management (HQACM): serious adverse events. Trial comparisons, record NCT00032591-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00032591-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 10.1690.150.189wilson
Risk in group 20.1720.1530.192wilson
Risk difference, group 1 minus group 2-0.00298-0.03030.0243newcombe hybrid score
Risk ratio, group 1 over group 20.9830.8371.15log
Odds ratio, group 1 over group 20.9790.8071.19log
Number needed to treat, for one fewer participant with a serious adverse event on Patient Self-Testing (PST) than on High Quality Anticoagulation Management (HQACM)335from 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 1Patient Self-Testing (PST)Patient Self-Testing (PST) of prothrombin time by international normalized ratio (PT-INR or INR) with weekly testing2471,465EG000
Group 2High Quality Anticoagulation Management (HQACM)High quality anticoagulation management (HQACM) with conventional monthly testing2501,457EG001

Harm

What it counts
Total, serious adverse events
Time frame
Full length of follow-up

Source ClinicalTrials.gov

Trial

Title
The Home INR Study
NCT number
NCT00032591
Phases
PHASE4
Conditions
Atrial Fibrillation
Interventions
Weekly patient self-testing of prothrombin time, High quality anticoagulation management (HQACM) with conventional monthly testing
Lead sponsor
US Department of Veterans Affairs
Results first posted
2014-02-06

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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