Rejuvenation.
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: Individuals in the study group for rejuvenation will undergo Q-switched laser therapy over three sessions (at baseline, one month later, and thr
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: Ages between 30-70 years.
Exclusion criteria
Exclusion criteria: History of keloid formation History of clotting disorders or the use of medications that affect clotting Uncontrolled diabetes or hypertension Active herpes infection in the lip area within the past month Lack of willingness or ability to attend follow-up appointments as scheduled History of hereditary or acquired connective tissue diseases History of skin cancer in the past 5 years Unrealistic expectations Use of other lip rejuvenation methods, including filler injections Allergy to lidocaine or tetracaine Fitzpatrick skin type >III History of lichen planus Lip shading and lip tattoo
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Hypopigmentation. Timepoint: starting the study, one month later, three months later. Method of measurement: Comparison of the before and after photos.;Hypopigmentation. Timepoint: starting the study, one month later, three months later. Method of measurement: Comparison of the before and after photos.;Scar. Timepoint: starting the study, one month later, three months later. Method of measurement: Comparison of the before and after photos. | — |
Primary
| Measure | Time frame |
|---|---|
| Lip volume improvement amount. Timepoint: Entering study, one month later, three months later. Method of measurement: Comparison of the before and after image.;Improving lip color. Timepoint: Entering study, one month later, three months later. Method of measurement: Comparison of the before and after image.;Improving lip texture. Timepoint: Entering study, one month later, three months later. Method of measurement: Comparison of the before and after image.;Side effects. Timepoint: Entering study, one month later, three months later. Method of measurement: Asking the patient and recording in the checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Samadi
Shahid Beheshti University of Medical Sciences
Outcome results
None listed