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Efficacy and Safety of a Preparation Containing an Antibiotic and Anti-Inflammatory Agent in Acne Vulgaris

Topical Clindamycin Salicylic Acid Preparation for the Treatment of Acne Vulgaris

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00361322
Enrollment
40
Registered
2006-08-08
Start date
2005-04-30
Completion date
2006-01-31
Last updated
2006-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acne Vulgaris

Brief summary

The concept behind our study was to combine an effect of antibiotic and anti-inflammatory agents for a more efficient acne therapy directed at the factors involved in the pathophysiology of the disease. For this purpose we evaluated a combination of clindamycin phosphate and salicylic acid in a non-irritating carrier.

Interventions

Sponsors

Hadassah Medical Organization
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years

Inclusion criteria

* mild to moderate acne vulgaris; * at least 5 lesions on the face; * a one-month wash-out period was established for any topical or systemic drug use for treatment of acne vulgaris.

Exclusion criteria

* acne that was primarily truncal, nodular, or due to secondary causes/internal disease; * pregnancy, breastfeeding, or intention to become pregnant; * another dermatological disease of the face; * significant systemic disease; * any drug/alcohol addiction; * interacting medication; * known hypersensitivity to study medications; * history of chronic disease treated with medications which might affect acne condition and treatment outcome (e.g. corticosteroids, lithium, isoniazid, anti-androgens, phenytoin, phenobarbital) in the preceding month

Design outcomes

Primary

MeasureTime frame
Lesions count at the baseline (week 0)
Lesions count at the end of study (week 8)

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026