Assessing effectiveness of PRP and tranexamic acid + vitamne C mesotherapy in the treatment of periorbital dark circle
Phase 2
- Conditions
- Periorbital hyperpigmentation.Other melanin hyperpigmentationL81.4
- Registration Number
- IRCT20200623047891N2
- Lead Sponsor
- Kerman University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Diagnosis of non-structural POH by dermatologist in Afzalipour hospital dermatology clinic
Filling the written letter of satisfaction to participate in the project
Minimum age of 18 when filling the letter of satisfaction
Male or non-pregnant, non-breast feeding female gender
Exclusion Criteria
Smoking
Previous or current bleeding disorders
Using anti coagulant medications
Presence of any active lesion in the treatment area
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of periorbital hyperpigmentation. Timepoint: At the begining of the study (before intervention) and 1 and 3 months after intervention. Method of measurement: Using Patient and Physician Global Assessment score.
- Secondary Outcome Measures
Name Time Method