Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue
Conditions
Interventions
Intervention1: Nil: Nil
Intervention2: Nil: Nil
Intervention3: Nil: Nil
Intervention4: Nil: Nil
Sponsors
NIL
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion Criteria 1. Age 12 years and above. 2. Patients with Fitzpatrick skin types three, four, five and six. 3. Patients with clinically diagnosed acne scars for example atrophic, hypertrophic, or mixed. 4. Willingness to participate and provide Informed Consent.
Exclusion criteria
Exclusion criteria: Exclusion Criteria 1. Patients with Fitzpatrick skin types one or two. 2. Patients with secondary causes of scarring other than acne for example trauma ,surgery ,burns ,varicella ,other dermatoses. 3. Pregnant & lactating patients. 4. Patients unwilling to participate and provide Informed Consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| co-primary objectives assessed at baseline in patients of skin of colour i.e Fitzpatrick 3to6 1To estimate the prevalence of acne scars. 2To estimate the associated risk factors of acne scars. 3To observe the clinical features ,types, grades, severity of acne scars using scoring systems like Goodman Baron qualitative scale and quantitative scale, qualitative global acne scarring grading system. 4To observe Psychological impact via Dermatology life quality index,The Cardiff Acne Disability Index.Timepoint: It is a cross sectional study | — |
Secondary
| Measure | Time frame |
|---|---|
| B. Secondary objectives to be assessed at baseline 1. To observe efficacy & safety of various therapeutic treatment modalities by grading of acne scars with the help of baseline & post procedural clinical examinations, objectively by using validated scoring systems like Goodman Baron qualitative & Goodman Baron quantitative scale & subjectively by using psychological impact assessment questionnaires like Dermatology life quality index, The Cardiff Acne Disability Index.Timepoint: It is a cross sectional study;2. To observe and record adverse events occurring, if any, in patients with the respective standard of care procedures planned for their treatment.Timepoint: It is a cross sectional study | — |
Countries
India
Contacts
Public ContactDr Nayan H Patel
GCS Medical College Hospital and Research Centre
Outcome results
None listed