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The goal of this randomized control trial is to compare the use of fractional carbon dioxide (Co2) laser to topical corticosteroids to treat lichen simplex chronicus (LSC) patients presenting to Dermatology outpatient clinic, Faculty of Medicine, Cairo University.
Participants will:
Researchers will divide and compare groups as follows:
Sixty patients will be divided randomly through closed envelop technique into 2 groups (Group A and B) each of 30 patients. Group A will be subdivided into 2 groups (1 and 2). All LSC lesions will be treated in any patient having multiple lesions.
to see if:
improve more in which group of patients after treatment.
Full description
All the patients were subjected to the following:
I. Before treatment:
A. Consent: An informed written consent will be signed by each patient before enrolment in the study.
B. Detailed history taking :
• Personal history: name, age, sex, skin type, occupation, residence, marital status, and smoking.
C. Skin biopsy: Two 3 mm punch biopsies will be taken from the lesion from each patient under local anesthesia using (Lidocaine®). One for histopathology to confirm diagnosis of LSC and the other for measuring itching mediators in the lesion before treatment by enzyme-linked immunosorbent assay (ELISA)). Another biopsy will be taken from a non lesional skin from same patient for measuring itching mediators by ELISA. Biopsies for ELISA will be stored at -20 degree celsius in eppendorfs with 3 ml phosphate buffer saline (PBS) added to each eppendorf. Tissue samples with PBS will be homogenized by a grinder, then centrifuged for 20 minutes at 3000 revolutions per minute (rpm) speed, the supernatant will be removed to be added to the ELISA kit wells for Human Interleukin-31, Nerve Growth Factor and Substance P assays (itching mediators)
D. Clinical assessment:
Pruritus severity scale.
Scaling, erythema, lichenification excoriation scores
Visual analogue scale.
Investigator's Global Assessment.
E. Depression assessment: Beck Depression Inventory questionnaire will be used to assess the depression in each patient .
F. Therapeutic Intervention: Patients will be divided as discussed before. - Topical steroids used will be a moderate potency topical steroid.
II. After treatment:
A. Assessment of biochemical efficacy (measuring itching mediators after treatment): After one month from the last session for group A and after one month from stoppage of steroids for group B, a skin biopsy from the plaque (from a nearby site to the former one) will be taken as discussed before for ELISA.
B. Assessment of clinical efficacy by scores as discussed before.
C. Depression assessment: Beck Depression Inventory questionnaire will be repeated.
D. Assessment of safety:
Erythema, burning sensation, PIH, pruritus and/or pixilation. • Assessment of side effects of topical corticosteroids and their treatment: Atrophy, telangiectasia, hypopigmentation, hypertrichosis, purpura, ulceration, irritation, secondary infection.
• Assessment of side effects of skin biopsy and their treatment: Bleeding, secondary infection and/or Scarring.
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60 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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