Comparison of the efficacy of botulinum toxin and triamcinolone in patients with hypertrophic scars treated with PDL laser
- Conditions
- Hypertrophic erythematous scar.Hypertrophic scarL91.0
- Registration Number
- IRCT20220121053776N1
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 12
Patients over 18 years
Patients with a confirmed diagnosis of hypertrophic erythematous scars of at least 3
The size of the mentioned lesions should be at least 10 × 10 cm or have a length of at least 10 cm
The patient is not pregnant or breast feeding
The patient has not received any treatment for lesions such as laser, topical or injectable corticosteroids in the past two months
The patient has no underlying diseases that lead to the healing process of the scar; Such as diabetes or weakened immune system
The patient's cooperation in performing medical interventions and referring to all treatment sessions
Occurrence of pregnancy during treatment or follow-up period
The occurrence of allergies or any side effects to one of the therapeutic interventions that prevent further treatment
Diagnosis of malignancy or systemic disease during treatment or follow-up period
The appearance of bacterial or viral skin diseases during treatment or follow-up
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effectiveness of treatment. Timepoint: Three months after the first treatment session. Method of measurement: By using Vancouver scar scale (VSS) scoring method.
- Secondary Outcome Measures
Name Time Method Safety. Timepoint: One, two and three months after the first treatment session. Method of measurement: Questions about possible side effects of treatment.;Tolerability. Timepoint: One, two and three months after the first treatment session. Method of measurement: Question from the patient.;Satisfaction. Timepoint: One, two and three months after the first treatment session. Method of measurement: Based on patient scoring.