None listed
Conditions
Brief summary
Acne vulgaris (AV) is a highly prevalent skin disorder which can be addressed through a range of therapies. Glycolic acid (GA) and salicylic acid (SA) represent two frequently utilized chemical peeling agents in acne therapy. Limited head-to-head comparative data on the efficacy of GA and SA peels as mono therapy is available especially in local population of Pakistan. This warrants conductance of this trial
Interventions
Sponsors
Study design
Eligibility
Inclusion criteria
- Patients clinically diagnosis of mild to moderate AV as per operational definition. - Bilateral, comparable facial involvement (which is a need for split-face randomization). - Patients willing to avoid any concurrent acne therapies throughout the trial. - No prior history of chemical peels in the past 6 months. - No use of systemic acne therapy within 3 months. - Agreed to provide written informed consent (guardian consent in case of minors).
Exclusion criteria
- Severe or nodulocystic acne, (predominantly truncal acne, or facial involvement) not suitable for split-face design. - Known allergy/intolerance to treatment ingredients (glycolic acid, salicylic acid, aspirin/salicylates, or other peel components). - Active facial dermatoses/infections (e.g., eczema, psoriasis, impetigo, fungal infection. - Pregnancy or lactation. - Active skin infections or dermatitis. - History of keloids or hypertrophic scarring. - Uncontrolled systemic disease (e.g., diabetes with poor control), use of immunosuppressive agents, or systemic retinoid use (within 6 months).