Herbal extract solution in treatment of seborrheic dermatitis

Phase 2

• Conditions: Seborrheic Dermatitis.; Other seborrhoeic dermatitis

• Registration Number: IRCT2015012520802N1
• Lead Sponsor: Vice chancellor for research,Islamic Azad University Pharmaceutical Branch of Tehran

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Male
• Target Recruitment: 20

Inclusion Criteria

male patients; healthy general condition; clinically diagnosed seborrheic dermatitis; 20-30 years old; consent form signed by patients.
Exclusion criteria:
use of topical steroids during 2 weeks ago; use of topical retinoids during 2 weeks ago; use of topical antifungals during 2 weeks ago; use oftopical anti-inflammatory druds during 2 weeks ago; use of topical antibiotics and any other topical treatments for seborrheic dermatitis like anti-dandruff shampoo and coal tar during 2 weeks ago; use of systemic anti-fungals during the last month; use of systemic steroids during the last month; use of systemic antibiotic during the last month; use of systemic anti-inflammatory drugs and immunomodulator drugs during the last month; use oral retinoid during last 6 months; history of hypersensitivity to azoles or herbal compound of our solution; comorbidities(AIDS,Parkinson,diabetes,…); skin disease like psoriasis, acne, …

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Scalp sebum. Timepoint: Beginning of the study, 2 weeks and 4 weeks after starting the treatment. Method of measurement: Sebometer.;Scalp PH. Timepoint: Beginning of the study, 2 weeks and 4 weeks after starting the treatment. Method of measurement: PH meter.;Dandruff. Timepoint: Beginning of the study, 2 weeks and 4 weeks after starting the treatment. Method of measurement: Pixel.

Secondary Outcome Measures

Name	Time	Method
Erythema and itching. Timepoint: Begining of the study,2 weeks and 4 weeks after treatment. Method of measurement: Clinical examination, Questionnaire.