IRCT20220121053776N1
Recruiting
Phase 2
Evaluation of the efficacy, safety, satisfaction and tolerability of treatment with diluted botulinum toxin A in comparison with intralesional triamcinolone in patients undergone PDL laser for Hypertrophic erythematous scars: A blinded randomized controlled clinical trial
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Iran University of Medical Sciences
- Enrollment
- 12
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Exclusion Criteria
- •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
Outcomes
Primary Outcomes
Not specified
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