ConductScience.org, home

Trial · NCT02800148

Bioequivalence Study of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea on the Face

NCT02800148, Phase 3, Completed, Padagis LLC; results first posted 2020-12-09

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Bioequivalence Study of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea on the Face. Trials, record NCT02800148. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02800148

On this page

Trial

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

Title
Bioequivalence Study of Two Treatments in the Treatment of Inflammatory Lesions of Rosacea on the Face
NCT number
NCT02800148
Status
Completed
Phases
Phase 3
Enrollment
667 participants, actual
Lead sponsor
Padagis LLC
Conditions
Rosacea
Interventions
Azelaic acid foam, Azelaic acid foam, Azelaic acid foam - Placebo
First posted
2016-06-15
Last updated
2021-11-08
Results first posted
2020-12-09

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryPercent Change (Reduction) of Lesion Count From Day 1Day 84

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercent Change (Reduction) of Lesion Count From Day 1Day 84percentage of lesion reductionMEAN

Results by group3

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

OutcomeGroupCategoryValueSpreadUnits
Percent Change (Reduction) of Lesion Count From Day 1Azelaic Acid Foam61.14Standard Deviation 33.623percentage of lesion reduction
Percent Change (Reduction) of Lesion Count From Day 1Finacea Foam57.27Standard Deviation 34.513percentage of lesion reduction
Percent Change (Reduction) of Lesion Count From Day 1Placebo Foam49.43Standard Deviation 44.437percentage of lesion reduction

Participant flow9

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDAzelaic Acid Foam224
Overall StudySTARTEDFinacea Foam224
Overall StudySTARTEDPlacebo Foam219
Overall StudyCOMPLETEDAzelaic Acid Foam199
Overall StudyCOMPLETEDFinacea Foam204
Overall StudyCOMPLETEDPlacebo Foam194
Overall StudyNOT COMPLETEDAzelaic Acid Foam25
Overall StudyNOT COMPLETEDFinacea Foam20
Overall StudyNOT COMPLETEDPlacebo Foam25

Adverse events12

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

TypeEventOrgan systemGroupAffectedAt riskEvents
seriousEsophageal CancerNeoplasms benign, malignant and unspecified (incl cysts and polyps)Azelaic Acid Foam1224
seriousEsophageal CancerNeoplasms benign, malignant and unspecified (incl cysts and polyps)Finacea Foam0224
seriousEsophageal CancerNeoplasms benign, malignant and unspecified (incl cysts and polyps)Placebo Foam0219
seriousAseptic MeningitisInfections and infestationsAzelaic Acid Foam0224
seriousAseptic MeningitisInfections and infestationsFinacea Foam0224
seriousAseptic MeningitisInfections and infestationsPlacebo Foam1219
seriousMajor DepressionPsychiatric disordersAzelaic Acid Foam0224
seriousMajor DepressionPsychiatric disordersFinacea Foam0224
seriousMajor DepressionPsychiatric disordersPlacebo Foam1219
seriousSuicidal ideationPsychiatric disordersAzelaic Acid Foam0224

Adverse event totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityAzelaic Acid Foam0224
Total, all-cause mortalityFinacea Foam0224
Total, all-cause mortalityPlacebo Foam0219
Total, other adverse eventsAzelaic Acid Foam0224
Total, other adverse eventsFinacea Foam0224
Total, other adverse eventsPlacebo Foam0219
Total, serious adverse eventsAzelaic Acid Foam1224
Total, serious adverse eventsFinacea Foam0224
Total, serious adverse eventsPlacebo Foam2219

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/NCT02800148

GET https://conductscience.org/api/trials/v1/NCT02800148/registered