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Phase 4 Completed N=33 Randomized Single-blind Treatment

Comparative Efficacy and Safety of Benzoyl Peroxide Used in Combination With Clindamycin vs. Benzoyl Peroxide Used in Combination With Clindamycin and Doxycycline in the Treatment of Moderate Acne

Source: ClinicalTrials.gov NCT00837213 ↗
Enrolled (actual)
33
Serious AEs
0.0%
Results posted
Aug 2010
Primary outcomePrimary: Percent Change in Inflammatory Acne Lesions From Baseline to Week 16 — -52.70; -48.84 Percent change

Summary

To compare the efficacy and safety of Benzoyl peroxide used in combination with clindamycin vs. Benzoyl peroxide used in combination with clindamycin and doxycycline in the treatment of moderate acne

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent Change in Inflammatory Acne Lesions From Baseline to Week 16
-52.70; -48.84
PRIMARY
Percent (%) Change in Non-inflammatory Acne Lesions From Baseline to Week 16.
-25.27; -44.69
PRIMARY
Percent Change in Total Acne Lesion Counts From Baseline to Week 16
-38.49; -46.11
PRIMARY
Change in Investigator Global Assessment (IGA)
-0.42; -0.61; -0.55; -0.85; -1; -1.09
SECONDARY
Percent (%) Change in Inflammatory Lesion Counts (Chest and Back) From Baseline to Week 12
-49.04; -45.44
SECONDARY
Percent Change in Non-inflammatory Lesions (Chest and Back) From Baseline to Week 12
-38.43; -38.52
SECONDARY
Percent Change in Total Lesions (Chest and Back) From Baseline to Week 12
-44.16; -41.74
SECONDARY
Percentage of Particpants With IGA Score at Week 16
0; 8.3; 0; 8.3; 30; 25

Eligibility Criteria

Inclusion Criteria

  • Male or female subjects with acne vulgaris . Able to understand the requirements of the study and sign informed consent/HIPAA authorization forms.

Exclusion Criteria

  • Known hypersensitivity to any of the components of the study drugs or used of prohibited medications or any medical condition that contraindicate the subject's participation in the clinical study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00837213). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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