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Comparison · NCT04893577-deaths

Study Drug (EDTA Eye Drops) vs Active Comparator (Abreva): deaths from any cause

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. Study Drug (EDTA Eye Drops) vs Active Comparator (Abreva): deaths from any cause. Trial comparisons, record NCT04893577-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04893577-deaths

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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 1000.434wilson
Risk in group 2000.434wilson
Risk difference, group 1 minus group 20-0.4340.434newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harmfrom the risk difference intervalthe two groups' risks are equal

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Study Drug (EDTA Eye Drops)Patients will treat herpes simplex eruption with EDTA eye drops.~EDTA: Patients will treat their cold sore with EDTA eye drops based upon their randomization.05EG000
Group 2Active Comparator (Abreva)Patients will treat herpes simplex eruption with Abreva.~Abreva: Patients will treat their cold sore with Abreva based upon their randomization05EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were collected over 12 days from beginning of randomization to end of study and 2 day follow-up call.

Source ClinicalTrials.gov

Trial

Title
EDTA Eye Drops Compared to Abreva for Herpes Simplex Virus Eruptions
NCT number
NCT04893577
Phases
PHASE2
Conditions
Herpes Simplex Oral
Interventions
EDTA, Abreva
Lead sponsor
University of Utah
Results first posted
2025-10-31

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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