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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04470466
Other study ID # las49
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 19, 2020
Est. completion date October 12, 2020

Study information

Verified date October 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Facial pores are visible topographic features of the skin that reflect openings of pilosebaceous follicles, that may be enlarged causing distress to some individuals. Many patients desire treatment for this condition, which can be an early sign of skin aging. Therapeutic modalities include intense pulsed light, radiofrequency, dermabrasion, oral and topical retinoids, as well as chemical peeling. Lasers, as fractional CO2, short pulse and Q-switched Nd-YAG, can potentially be used in treatment of wide pores. This study aims at the assessment and comparison of therapy with short pulsed and Q-switched Nd-YAG laser plus topical carbon with fractional CO2 laser in the management of wide facial pores.


Description:

topical carbon cream will be applied to one side of the face in patients with wide facial pores, followed by 2 passes of short pulse 1064 ND:YAG laser, then one pass of Q-switched ND-YAG laser. fractional CO2 laser will be performed to the other half of the face. the patients will receive 2 treatment sessions


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date October 12, 2020
Est. primary completion date October 12, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - Participants who are more than 18 years old with the large facial pores and are aware of their problem and seeking treatment Exclusion Criteria: - • Previous laser therapy, chemical peeling, microdermabrasion or cosmetic procedure for the face. - Patients with any contraindication to laser therapy such as photosensitive diseases, skin malignancies, patients on oral retinoids. - Keloid-forming tendency. - Local or systemic treatment for skin pores in the previous 3 months - Connective tissue disease or the use of immunosuppressive medications. - Pregnancy. - Present or past history of herpes labialis.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
short pulse and Q-switched ND-YAG laser with topical carbon
application of topical carbon cream, followed by two passes of short pulse 1064 ND-YAG, then one pass of Q-switched 1064 ND-YAG on one side of the face
fractional CO2 laser
single pass of fractional CO2 laser on the other side of the face

Locations

Country Name City State
Egypt Kasr Alainy Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the percentage of decrease in size of enlarged facial pores assessed clinically and by dermoscopy 2 months
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