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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
Tel-Aviv Sourasky Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Keloid

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    July 29, 2020
    Last Updated
    October 18, 2020
    Sponsor
    Tel-Aviv Sourasky Medical Center
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    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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