Evaluation of the effect of glycyrrhizin hydrogel on laser burns

Phase 3

Recruiting

• Conditions: aser induced dermatitis.; Other specified disorders of the skin and subcutaneous tissue related to radiation; L59.8

• Registration Number: IRCT20191106045356N17
• Lead Sponsor: Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Clients starting to use laser
Clients aged 18 to 55 years
No history of licorice allergy
Absence of severe systemic disease such as uncontrolled diabetes, epilepsy, immune system deficiency, etc.
Willingness to participate in the study and complete the ethical consent form

Exclusion Criteria

Clients with skin disease
Allergy to glycyrrhizin or any of the compounds used
Exacerbation of dermatitis or 2nd degree burns
Non-cooperation of the volunteer in using medicine for more than one day

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Grading the intensity of skin redness. Timepoint: After starting treatment at times 1, 2, 4, 7, 10, 15. Method of measurement: The condition of the laser site in terms of the loss of the epidermis, the intensity of redness, dryness, itching, burning, and pain (based on the visual analog scale), and the patient's satisfaction with the use of the drug, and that the skin of the laser area has undergone second-degree burns. are evaluated or not, as well as the need to use the standard treatment of dermatitis.