Comparison of the Efficacy of Different Steroids in the Treatment of Abnormal Scars (Keloids, Hypertrophic Scars)
Primary Purpose
Keloid, Hypertrophic Scar, Scars
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Betamethasone acetate + Betamethasone sodium phosphate
Dexamethasone sodium phosphate
Methylprednisolone acetate
Triamcinolone acetonide
Sponsored by
About this trial
This is an interventional treatment trial for Keloid
Eligibility Criteria
Inclusion Criteria:
- 20 participants with at least 4 keloids
- 20 participants with a hypertrophic scar of at least 11 cm length
Exclusion Criteria:
- current or planned pregnancy
- breastfeeding women
- participants suffering from diabetes mellitus or coagulation disorders
- infection at planned injection sites
- systemic treatment of corticosteroids, 5-fluorouracil
- known allergy to any of the following: Betamethasone acetate + Betamethasone sodium phosphate, Triamcinolone acetonide, Dexamethasone sodium phosphate, Methylprednisolone acetate
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
keloids
hypertrophic scars
Arm Description
each patient will be injection by all 4 steroids for comparison patients with 4 or more keloids will be injection with each steroid for different keloid
each patient will be injection by all 4 steroids for comparison patients with a 11 cm hypertrophic scar will be injected by all 4 steroids along the scar with a 1 cm distance between each steroid
Outcomes
Primary Outcome Measures
Patient and Observer Scar Assessment Scale (POSAS)
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Patient and Observer Scar Assessment Scale (POSAS)
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Patient and Observer Scar Assessment Scale (POSAS)
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Secondary Outcome Measures
Visual analogue scale (pain scale)
1 - paineless, 10- extremely painfull
Dermatologist's assessment
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
3D camera
improvement percentage of scar volume
Participant's assessment
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Dermatologist's assessment
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
3D camera
improvement percentage of scar volume
Participant's assessment
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Full Information
NCT ID
NCT04593706
First Posted
July 29, 2020
Last Updated
October 18, 2020
Sponsor
Tel-Aviv Sourasky Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT04593706
Brief Title
Comparison of the Efficacy of Different Steroids in the Treatment of Abnormal Scars (Keloids, Hypertrophic Scars)
Official Title
Comparison of the Efficacy of Different Steroids in the Treatment of Abnormal Scars (Keloids, Hypertrophic Scars)
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2020 (Anticipated)
Primary Completion Date
October 31, 2021 (Anticipated)
Study Completion Date
October 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Tel-Aviv Sourasky Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Comparison of the Efficacy of Different Steroids in the Treatment of Abnormal Scars (Keloids and hypertrophic Scars)
Detailed Description
On a yearly basis, millions develop different skin scarring. These scars are a public reminder of the traumatic incident, past or present disease or a surgery which caused them.
Scarring is a common consequence of wound healing process, and it is one of the most complex biological processes in human. This healing process is affected by numerous factors and thus can be disrupted, leading to pathological scarring.
Pathological scarring is common in people with genetic predisposition, those undergone complex and massive surgeries, burns or those wounded in unsanitary environments. Apart from being aesthetically unpleasant, scars are associated with functional and psychosocial morbidities.
Despite clinical, pathologic and pathogenic differences between keloids and hypertrophic scars, treatments are similar.
Scars have a negative external impact causing social distress and impaired self-image, and as a consequence, low satisfaction rates following surgical and cosmetic procedures.
The first line treatment is monthly intralesional corticosteroid injections with a response rate of 50-100% and recurrence of 50%.
There are a few steroids available and used for abnormal scars treatment, including Celestone chronodose (Betamethasone acetate + Betamethasone sodium phosphate), Dexamethasone sodium phosphate, Methylprednisolone acetate, Methylprednisolone sodium succinate, Methylprednisolone hemisuccinate, Triamcinolone acetonide.
Steroids are different by their hydrophilic properties, potency and half-life, although the half-life of intralesional injections is not known. Inspite of being widely used, there have never been a comparative study of the different steroid treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Keloid, Hypertrophic Scar, Scars, Scarring
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
keloids
Arm Type
Active Comparator
Arm Description
each patient will be injection by all 4 steroids for comparison patients with 4 or more keloids will be injection with each steroid for different keloid
Arm Title
hypertrophic scars
Arm Type
Active Comparator
Arm Description
each patient will be injection by all 4 steroids for comparison patients with a 11 cm hypertrophic scar will be injected by all 4 steroids along the scar with a 1 cm distance between each steroid
Intervention Type
Drug
Intervention Name(s)
Betamethasone acetate + Betamethasone sodium phosphate
Intervention Description
the steroid will be injected to either a keloid or a 1.5 c"m of the 11 c"m hypertrophic scar
Intervention Type
Drug
Intervention Name(s)
Dexamethasone sodium phosphate
Intervention Description
the steroid will be injected to either a keloid or a 1.5 c"m of the 11 c"m hypertrophic scar
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone acetate
Intervention Description
the steroid will be injected to either a keloid or a 1.5 c"m of the 11 c"m hypertrophic scar
Intervention Type
Drug
Intervention Name(s)
Triamcinolone acetonide
Intervention Description
the steroid will be injected to either a keloid or a 1.5 c"m of the 11 c"m hypertrophic scar
Primary Outcome Measure Information:
Title
Patient and Observer Scar Assessment Scale (POSAS)
Description
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Time Frame
enrollment, data will be reported through study completion an average of 1 year
Title
Patient and Observer Scar Assessment Scale (POSAS)
Description
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Time Frame
3 months post last treatment, data will be reported through study completion an average of 1 year
Title
Patient and Observer Scar Assessment Scale (POSAS)
Description
For the Observer Scar Assessment Scale (OSAS), the investigators score the following parameters of each part of the scar on a scale ranging from 1 (normal skin) to 10 (worst scar imagin¬able): 'vascularization', 'pigmentation', 'thickness', 'relief', and 'pliability'. The total score on the OSAS is the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst). For the patient scar assessment scale (PSAS), the participants used a scale of 1 to 10 to answer questions relating to pain, itching, color, stiffness, irregularity and thickness. The total score on the PSAS was the sum of the scores of each item, yielding a total score ranging from 6 (best) to 60 (worst)
Time Frame
6 months post last treatment, data will be reported through study completion an average of 1 year
Secondary Outcome Measure Information:
Title
Visual analogue scale (pain scale)
Description
1 - paineless, 10- extremely painfull
Time Frame
at each of the three treatment appointments, data will be reported through study completion an average of 1 year
Title
Dermatologist's assessment
Description
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Time Frame
3 months post last treatment, data will be reported through study completion an average of 1 year
Title
3D camera
Description
improvement percentage of scar volume
Time Frame
3 months post last treatment, data will be reported through study completion an average of 1 year
Title
Participant's assessment
Description
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Time Frame
3 months post last treatment, data will be reported through study completion an average of 1 year
Title
Dermatologist's assessment
Description
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Time Frame
6 months post last treatment, data will be reported through study completion an average of 1 year
Title
3D camera
Description
improvement percentage of scar volume
Time Frame
6 months post last treatment, data will be reported through study completion an average of 1 year
Title
Participant's assessment
Description
0- no change, 1-minor change <5%, 2-Mild change - 25-50%, 3- Moderate Change 50-75%, 4-Significant change > 75%
Time Frame
6 months post last treatment, data will be reported through study completion an average of 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
20 participants with at least 4 keloids
20 participants with a hypertrophic scar of at least 11 cm length
Exclusion Criteria:
current or planned pregnancy
breastfeeding women
participants suffering from diabetes mellitus or coagulation disorders
infection at planned injection sites
systemic treatment of corticosteroids, 5-fluorouracil
known allergy to any of the following: Betamethasone acetate + Betamethasone sodium phosphate, Triamcinolone acetonide, Dexamethasone sodium phosphate, Methylprednisolone acetate
12. IPD Sharing Statement
Learn more about this trial
Comparison of the Efficacy of Different Steroids in the Treatment of Abnormal Scars (Keloids, Hypertrophic Scars)
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