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Comparison · NCT03154333-ceee39ad

Diacerein 1% Ointment vs Vehicle Ointment: The Proportion of Subjects Who Achieved Success on the Investigator's Global Assessment (IGA)

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. Diacerein 1% Ointment vs Vehicle Ointment: The Proportion of Subjects Who Achieved Success on the Investigator's Global Assessment (IGA). Trial comparisons, record NCT03154333-ceee39ad. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03154333-ceee39ad

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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 10.4290.2650.609wilson
Risk in group 20.2690.1370.461wilson
Risk difference, group 1 minus group 20.159-0.09250.383newcombe hybrid score
Risk ratio, group 1 over group 21.590.7413.42log
Odds ratio, group 1 over group 22.040.6486.4log
Number needed to treat, for one more participant with the outcome on Diacerein 1% Ointment than on Vehicle Ointment6.28from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: vehicle.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Diacerein 1% Ointmentdiacerein 1% ointment will be used for 8 weeks~diacerein 1% ointment: diacerein 1% ointment administered1228OG000
Group 2Vehicle Ointmentvehicle ointment will be used for 8 weeks~vehicle ointment administered topically726OG001

Outcome

Type
SECONDARY
Title
The Proportion of Subjects Who Achieved Success on the Investigator's Global Assessment (IGA)
Description
The investigator's global assessment (IGA) is a five-point scale that is used for overall clinical assessment of severity of disease and classifies EBS-involved skin with a score ranging from 0-4. Success on the IGA was defined as ≥2-point reduction from Baseline to Visit 6 (Week 8).~IGA Scoring:~0 = Clear; 1 = Near Clear; 2 = Mild; 3 = Moderate; 4 = Severe~Minimum score = 0 Maximum score = 4; higher score = worse outcome
Time frame
Baseline to Week 8
Population
All efficacy analyses were conducted using the Intent to Treat (ITT) Population that consisted of all randomized subjects who were dispensed study drug. Subjects were included in the treatment group to which they were assigned.

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Diacerein 1% Ointment for Subjects With Epidermolysis Bullosa Simplex (EBS)
NCT number
NCT03154333
Phases
PHASE2
Conditions
Epidermolysis Bullosa Simplex
Interventions
diacerein 1% ointment, A placebo ointment
Lead sponsor
Castle Creek Pharmaceuticals, LLC
Results first posted
2019-11-05

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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