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Trial · NCT02795117

Comparative Safety and Efficacy of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea

NCT02795117, Phase 3, Completed, Padagis LLC; results first posted 2021-01-05

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Comparative Safety and Efficacy of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea. Trials, record NCT02795117. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02795117

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Trial

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

Title
Comparative Safety and Efficacy of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea
NCT number
NCT02795117
Status
Completed
Phases
Phase 3
Enrollment
486 participants, actual
Lead sponsor
Padagis LLC
Conditions
Rosacea
Interventions
Ivermectin, Ivermectin (reference), Placebo
First posted
2016-06-09
Last updated
2021-11-02
Results first posted
2021-01-05

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryMean Percent Change From Baseline in the Inflammatory (Papules and Pustules) Lesion CountDay 1 to Day 84
SecondarySubjects With Clinical Success on the Investigator Global AssessmentDay 1 to Day 84Clinical success is defined as a score of clear or almost clear

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYMean Percent Change From Baseline in the Inflammatory (Papules and Pustules) Lesion CountDay 1 to Day 84Per protocol populationpercentage of lesion reductionMEAN
SECONDARYSubjects With Clinical Success on the Investigator Global AssessmentDay 1 to Day 84Per protocol populationParticipantsCOUNT_OF_PARTICIPANTS

Results by group6

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

OutcomeGroupCategoryValueSpreadUnits
Mean Percent Change From Baseline in the Inflammatory (Papules and Pustules) Lesion CountTest Product65.47Standard Deviation 30.222percentage of lesion reduction
Mean Percent Change From Baseline in the Inflammatory (Papules and Pustules) Lesion CountReference Product67.89Standard Deviation 30.244percentage of lesion reduction
Mean Percent Change From Baseline in the Inflammatory (Papules and Pustules) Lesion CountPlacebo55.51Standard Deviation 32.660percentage of lesion reduction
Subjects With Clinical Success on the Investigator Global AssessmentTest Product71Participants
Subjects With Clinical Success on the Investigator Global AssessmentReference Product79Participants
Subjects With Clinical Success on the Investigator Global AssessmentPlacebo26Participants

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDTest Product193
Overall StudySTARTEDReference Product193
Overall StudySTARTEDPlacebo100
Overall StudyCOMPLETEDTest Product175
Overall StudyCOMPLETEDReference Product166
Overall StudyCOMPLETEDPlacebo88
Overall StudyNOT COMPLETEDTest Product18
Overall StudyNOT COMPLETEDReference Product27
Overall StudyNOT COMPLETEDPlacebo12

Adverse events0

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

None in this release.

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityTest Product0193
Total, all-cause mortalityReference Product0193
Total, all-cause mortalityPlacebo0100
Total, other adverse eventsTest Product0193
Total, other adverse eventsReference Product0193
Total, other adverse eventsPlacebo0100
Total, serious adverse eventsTest Product0193
Total, serious adverse eventsReference Product0193
Total, serious adverse eventsPlacebo0100

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

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 comparisons0

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

None in this release.

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/NCT02795117

GET https://conductscience.org/api/trials/v1/NCT02795117/registered