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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05283876
Other study ID # Excimer light in psoriasis
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 10, 2022
Est. completion date March 30, 2023

Study information

Verified date February 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to determine the standard tissue levels of SP and its receptor in lesional skin of psoriasis patients in both developing and stationary stages before and after excimer light therapy.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date March 30, 2023
Est. primary completion date March 30, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Type of Psoriasis: plaque psoriasis. - Less than 10% surface area. Exclusion Criteria: - Erythrodermic psoriasis - Pustular psoriasis - Topical treatment for psoriasis for the past 2 weeks. - Systemic retinoids in the last 2 years. - Systemic treatments (including any drugs that affect SP level as Aprepitant) in the last 3 months. - Contraindications to excimer light therapy (history of skin malignancy or precancerous conditions like xeroderma pigmentosum or photosensitivity)

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Excimer light
Excimer light sessions

Locations

Country Name City State
Egypt Kasr Al Ainy Faculty of medicine Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Excimer laser efficiency in active and stable psoriasis Determine the clinical improvement using Local psoriasis severity index through study completion, an average of 6 months
Primary Excimer laser efficiency on neurogenic inflammation level of affection of the neurogenic inflammation in psoriasis lesions after using Excimer light therapy. Determine substance P and its receptor levels before and after therapy. through study completion, an average of 6 months
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