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Efficacy of brimonidine gel for the prevention of erythema and post inflammatory hyperpigmentation fallowing ablative CO2 laser

Evaluation of the efficacy of brimonidine gel for the prevention of erythema and post inflammatory hyperpigmentation fallowing ablative CO2 laser

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150825023753N29
Enrollment
28
Registered
2025-05-03
Start date
2025-04-26
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post laser hyperpigmentation. Postinflammatory hyperpigmentation

Interventions

Intervention 1: Intervention group: Patients will receive a combination formula (1:1 mixture of XYLA-P? and Janoberim?, ) on one side of the face, and after 30 minutes, each participant will receive a

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ??-?? years of age Patients with solar lentigo and freckles which is symmetrical on both sides of the face During the study, fertile women must be using effective contraception

Exclusion criteria

Exclusion criteria: Clinical active dermatological disease in the face• Wounds, dermatitis, tattoos or scars in treatment area• Current treatment with monoamine oxidase inhibitors, tricyclic or tetracyclic antidepressants which interacts with the noradrenergic transmission Current treatment with other systemic adrenergic receptor agonists or antagonists UV-exposure (solarium or sunbathing) or other treatment within the last month that enhances skin pigmentation Use of other topical agents that may interact with treatment Local or systemic treatment with photosensitizing drugs Pregnancy and breastfeeding women Current participation in other clinical trials Allergies to ingredients in birimonidine•

Design outcomes

Primary

MeasureTime frame
Post laser erythema. Timepoint: At the beginning of the study, then 30 minutes, 60 minutes, one month, and two months after receiving the interventions. Method of measurement: Clinician's Erythema Assessment (CEA).;The extent of post-laser inflammation-induced hyperpigmentation. Timepoint: One month and two months after receiving the interventions. Method of measurement: Physician clinical assessment and Likert scale.

Secondary

MeasureTime frame
Pain severity. Timepoint: During the laser procedure, immediately after, ?? minutes, ?? minutes after the procedure. Method of measurement: Likert scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mitra Abdolvand

Shiraz University of Medical Sciences

mitra.abd??@gmail.com+98 71 3212 5592

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026