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Trial · NCT04893577

EDTA Eye Drops Compared to Abreva for Herpes Simplex Virus Eruptions

NCT04893577, Phase 2, Completed, University of Utah; results first posted 2025-10-31

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. EDTA Eye Drops Compared to Abreva for Herpes Simplex Virus Eruptions. Trials, record NCT04893577. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04893577

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
EDTA Eye Drops Compared to Abreva for Herpes Simplex Virus Eruptions
NCT number
NCT04893577
Status
Completed
Phases
Phase 2
Enrollment
10 participants, actual
Lead sponsor
University of Utah
Conditions
Herpes Simplex Oral
Interventions
EDTA, Abreva
First posted
2021-05-19
Last updated
2025-10-31
Results first posted
2025-10-31

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryDuration (Days) of Herpes Labialis Outbreak Until HealedUp to 14 days per patientWe will measure the number of days until lesion is healed from start of lesion to lesion resolved.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYDuration (Days) of Herpes Labialis Outbreak Until HealedUp to 14 days per patientdaysMEAN

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Duration (Days) of Herpes Labialis Outbreak Until HealedStudy Drug (EDTA Eye Drops)10.6Full Range 8 to 13days
Duration (Days) of Herpes Labialis Outbreak Until HealedActive Comparator (Abreva)8.25Full Range 3 to 14days

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDStudy Drug (EDTA Eye Drops)5
Overall StudySTARTEDActive Comparator (Abreva)5
Overall StudyCOMPLETEDStudy Drug (EDTA Eye Drops)5
Overall StudyCOMPLETEDActive Comparator (Abreva)4
Overall StudyNOT COMPLETEDStudy Drug (EDTA Eye Drops)0
Overall StudyNOT COMPLETEDActive Comparator (Abreva)1

Adverse events2

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherBurning during application of study drugSkin and subcutaneous tissue disordersStudy Drug (EDTA Eye Drops)252
otherBurning during application of study drugSkin and subcutaneous tissue disordersActive Comparator (Abreva)050

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityStudy Drug (EDTA Eye Drops)05
Total, all-cause mortalityActive Comparator (Abreva)05
Total, other adverse eventsStudy Drug (EDTA Eye Drops)25
Total, other adverse eventsActive Comparator (Abreva)05
Total, serious adverse eventsStudy Drug (EDTA Eye Drops)05
Total, serious adverse eventsActive Comparator (Abreva)05

Papers8

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
1390034BACKGROUNDPubMed
9878012BACKGROUNDPubMed
10837169BACKGROUNDPubMed
12019102BACKGROUNDPubMed
12692270BACKGROUNDPubMed
12954137BACKGROUNDPubMed
14966254BACKGROUNDPubMed
24942591BACKGROUNDPubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons2

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource
Study Drug (EDTA Eye Drops) vs Active Comparator (Abreva): deaths from any causeTrial comparisons
Study Drug (EDTA Eye Drops) vs Active Comparator (Abreva): serious adverse eventsTrial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT04893577

GET https://conductscience.org/api/trials/v1/NCT04893577/registered