A Comparative Investigation of Efficacy and Complications in Light and Deep Chemical Peels

N/AActive Not RecruitingNCT06749561

Superior University112 enrolled

Overview

Chemical peeling involves applying substances to the skin to induce controlled damage, which promotes the regeneration of fresh skin cells and enhances the skin's appearance.

This study will be a cross-sectional analysis with a sample size of 112 patients.

Study Type

OBSERVATIONAL

Enrollment

112

Conditions

Peeling Skin Syndrome

Interventions

Group 1DIAGNOSTIC_TEST

To Compare the safety and effectiveness of boyh types

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 35 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy males and females aged 18-35 years. * Willing to provide informed consent and follow the treatment protocol. Exclusion Criteria: * Pregnant or breastfeeding women. * Active skin conditions (e.g., acne, eczema). * Use of medications that affect skin healing. * Known allergies to chemical peel substances.

Locations (1)

Block E3 E-3 Gulberg III

Lahore, Punjab Province, Pakistan

Outcomes

Primary Outcomes

Dermatological Assessment Score (DAS)

The area-wise percentage involvement of the involved sites is calculated as: 1 = less than 10% area; 2 = 10-29%; 3 = 30-49%; 4 = 50-69%; 5 = 70-89%; and 6 = more than 90%. The maximum score of PASI is 72. PASI 75 is a 75% reduction of baseline PASI score.

Time frame: 12 Months

Data from ClinicalTrials.gov

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