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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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8 January 2018 |
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Main ID: |
NCT02798016 |
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Date of registration:
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13/05/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Treatment of Atrophic Acne Scars With Platelet-Rich Plasma and Skin Needling
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Scientific title:
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Treatment of Atrophic Acne Scars With Platelet-Rich Plasma Alone or in Combination With Skin Needling: A Randomized Controlled Trial |
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Date of first enrolment:
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October 2015 |
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Target sample size:
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50 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02798016 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Single (Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Syrian Arab Republic
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Contacts
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Name:
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Faiez Al-Deghlaoui, MD MSc PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Associate Professor of Dermatology and Veneology, Medical School, University of Damascus |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Atrophic acne scars on both sides of the face
Exclusion Criteria:
- patients with active acne, herpes labialis, or bacterial infection; warts on the face,
actinic keratosis, or skin cancer
- systemic retinoids intake in the previous 6 months,
- diabetes, pregnancy, history of keloidal scarring; or patients with severe systemic
illness or malignancy
- patients on anticoagulant therapy or aspirin or have a coagulation issue,
- patients with hemoglobin less than 10g\dl or platelet less than 105 micron\l
- any previous procedures for acne scar within the last 6 months
Age minimum:
18 Years
Age maximum:
65 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Atrophic Acne Scars
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Intervention(s)
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Procedure: Micro-needling
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Procedure: Platelet-Rich Plasma
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Primary Outcome(s)
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Change in Scar Appearance
[Time Frame: Scar Appearance will be assessed at: T1; one day (wihtin 24 hours) before the application of the intervention(s); and T2: after three months of applying the intervention(s).]
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Secondary Outcome(s)
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Patients' Satisfaction
[Time Frame: This is going to be assessed six months following the application of the intervention and the active comparator]
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Secondary ID(s)
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UDMS-Dermat-01-2016
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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