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Comparison · NCT02158806-eaf8dd3a

Aspirin vs Placebo: Number of Participants With Healed Venous Leg Ulcers

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. Aspirin vs Placebo: Number of Participants With Healed Venous Leg Ulcers. Trial comparisons, record NCT02158806-eaf8dd3a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02158806-eaf8dd3a

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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 10.7040.6190.777wilson
Risk in group 20.8020.7230.862wilson
Risk difference, group 1 minus group 2-0.0976-0.2020.0093newcombe hybrid score
Risk ratio, group 1 over group 20.8780.7611.01log
Odds ratio, group 1 over group 20.5890.3291.05log
Number needed to treat, for one fewer participant with the outcome on Aspirin than on Placebo10.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Aspirin150 mg capsule once daily for up to 24 weeks~Aspirin: 150 mg aspirin in capsule form once daily for up to 24 weeks88125OG000
Group 2PlaceboMatching inert capsule once daily for up to 24 weeks~Placebo: Matching placebo capsule containing inert bulking agent101126OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Healed Venous Leg Ulcers
Description
Number of participants in each arm with completely healed reference ulcers at 24 weeks
Time frame
24 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Low Dose Aspirin for Venous Leg Ulcers
NCT number
NCT02158806
Phases
PHASE3
Conditions
Venous Leg Ulcer
Interventions
Aspirin, Placebo
Lead sponsor
University of Auckland, New Zealand
Results first posted
2019-01-04

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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