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Tolerance Assessment of Tailored 3d-printed TFO With Silicone Interface for the Treatment of Post-burn Face Scar (ECORCE)

Primary Purpose

Burn Scar

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
COFIS 3D
Sponsored by
Centre Hospitalier Régional Metz-Thionville
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Burn Scar focused on measuring Burns, Transparent Face Orthosis, Silicone application, 3d Printed, Face

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years
  • Post-Burn Face scar during maturation stage or surgical intervention on post-burn face scar during maturation stage
  • Patient agrees to shave beard if necessary for 3D camera measurement
  • Patient able to express informed consent
  • Affiliation to a social security scheme

Exclusion Criteria:

  • Post burn face scar in the sequela stage
  • Patient with unbalanced photosensitive epilepsy
  • Patient with an unconsolidated fracture of the face's bones or skull
  • Patient with a known allergy to silicone
  • Pregnant or lactating women

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Post-Burn Face scar

    Arm Description

    Use of 3d printed TFO with silicone interface (COFIS 3D)

    Outcomes

    Primary Outcome Measures

    Number of Local Side Effects
    wound, device related pain, rash, temporomandibular joint pain, dental pain, suffocating sensation

    Secondary Outcome Measures

    Evaluation of scar evolution with VSS
    Vancouver Scar Scale (VSS) assesses 4 variables: vascularity (range 0-3), height/thickness (range 0-3), pliability (range 0-5) and pigmentation (0-2). A total scores ranges from 0 to 13, whereby a score of 0 reflects normal skin.
    Evaluation of scar evolution with POSAS
    Evaluation of scar evolution by Patient and Observer Scar Assessment Scale (POSAS). It consists of two scales which assesses vascularity, pigmentation, thickness, relief, pliability, and surface area and it incorporates patient assessment of pain, itching, color, stiffness, thickness and relief. All items were evaluated on numerical rating scales ranging from 1 to 10 (with 10 indicating the worst score).
    Wearing time
    Diurnal and nocturnal wearing time in hours
    Manufacturing time
    Time of device's manufacturing
    Reprints
    Number of reprints needed per patient
    Device lifetime
    Device lifetime corresponds to the time between implementation and change of device (for any Reason) in days
    Evaluation of the quality of life with the BSHS-B
    Evaluation of the quality of life of patients by the BSHS-B (Burn Specific Health Scale - Brief). The BSHS-B consists of 40 items divided into four domains with nine subscales (heat sensitivity, affect, hand function, treatment regimens, work, sexuality, interpersonal relationships, simple abilities and body change). Items are answered on a 5-point Likert scale ranging from 0 (extremely) to 4 (not at all).
    Number of Local side effects
    wound, device related pain, rash, temporomandibular joint pain, dental pain, suffocating sensation

    Full Information

    First Posted
    February 25, 2021
    Last Updated
    May 3, 2023
    Sponsor
    Centre Hospitalier Régional Metz-Thionville
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04884789
    Brief Title
    Tolerance Assessment of Tailored 3d-printed TFO With Silicone Interface for the Treatment of Post-burn Face Scar
    Acronym
    ECORCE
    Official Title
    Tolerance Assessment of Tailored 3d-printed Transparent Face Orthosis With Silicone Interface for the Treatment of Post-burn Face Scar
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 1, 2023 (Anticipated)
    Primary Completion Date
    April 1, 2026 (Anticipated)
    Study Completion Date
    April 1, 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Centre Hospitalier Régional Metz-Thionville

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to assess the tolerance of tailored 3d-printed transparent face orthosis used in the medical care of post-burn face scar.
    Detailed Description
    Burn injuries are not a rare affection. According to WHO (World Health Organization), in 2004 there were 11 million peoples in the world who were affected by burn injuries caused by fire and who needed medical cares. This important number ignores non-fire thermal, chemical and electrical burns. Face is one of the most susceptible areas of burn where the prevalence was reported to be 6-60%. Hypertrophic scars (HS) are frequent consequences of dermal burn with a prevalence of 70% of burned people. HS, which are a dermal fibro-proliferation, are rigid, erythematous and thickened scars associated with pigmentation abnormalities, xerosis, thermal sensitivity, pain and pruritus. When HS is located on the face, they can cause cosmetic disorder with disfigurement and psychological distress. Pressure therapy and silicone application are the two recommended non-invasive care for prevention and treatment of hypertrophic scarring after burn. On the face, Pressure Garment Therapy (PGT) cannot exert the required pressure because of concave or flat shape so the use of face mask is the most common form of pressure therapy on the face. The face mask manufacturing is artisanal, time consuming and variable between all burn centers. They are not very accurate and have difficulties to apply effective pressure on certain face areas such as nasolabial folds. Our Transparent Face Orthosis (TFO) uses tri-dimensional cam for measurement and 3d-printing technology for manufacturing. We think this way to manufacture the TFO will be more accurate and efficient, less expansive and time consuming. Moreover, the addition of a silicone interface between the TFO and the face will associate silicone application therapy and pressure therapy what should be more effective than pressure therapy alone. The purpose of this study is to assess the tolerance of tailored 3d-printed transparent face orthosis used in the medical care of post-burn face scar.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Burn Scar
    Keywords
    Burns, Transparent Face Orthosis, Silicone application, 3d Printed, Face

    7. Study Design

    Primary Purpose
    Device Feasibility
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    13 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Post-Burn Face scar
    Arm Type
    Experimental
    Arm Description
    Use of 3d printed TFO with silicone interface (COFIS 3D)
    Intervention Type
    Device
    Intervention Name(s)
    COFIS 3D
    Other Intervention Name(s)
    3d printed Transparent Face Orthosis with silicone interface
    Intervention Description
    Patient have to wear the COFIS 3D 20h a day for at least 6 month
    Primary Outcome Measure Information:
    Title
    Number of Local Side Effects
    Description
    wound, device related pain, rash, temporomandibular joint pain, dental pain, suffocating sensation
    Time Frame
    Month 1
    Secondary Outcome Measure Information:
    Title
    Evaluation of scar evolution with VSS
    Description
    Vancouver Scar Scale (VSS) assesses 4 variables: vascularity (range 0-3), height/thickness (range 0-3), pliability (range 0-5) and pigmentation (0-2). A total scores ranges from 0 to 13, whereby a score of 0 reflects normal skin.
    Time Frame
    Month 1; Month 6; Month 12; Month 18; Month 24
    Title
    Evaluation of scar evolution with POSAS
    Description
    Evaluation of scar evolution by Patient and Observer Scar Assessment Scale (POSAS). It consists of two scales which assesses vascularity, pigmentation, thickness, relief, pliability, and surface area and it incorporates patient assessment of pain, itching, color, stiffness, thickness and relief. All items were evaluated on numerical rating scales ranging from 1 to 10 (with 10 indicating the worst score).
    Time Frame
    Month 1; Month 6; Month 12; Month 18; Month 24
    Title
    Wearing time
    Description
    Diurnal and nocturnal wearing time in hours
    Time Frame
    Month 1; Month 6; Month 12; Month 18; Month 24
    Title
    Manufacturing time
    Description
    Time of device's manufacturing
    Time Frame
    Month 1; Month 6; Month 12; Month 18; Month 24
    Title
    Reprints
    Description
    Number of reprints needed per patient
    Time Frame
    Month 1; Month 6; Month 12; Month18; Month 24
    Title
    Device lifetime
    Description
    Device lifetime corresponds to the time between implementation and change of device (for any Reason) in days
    Time Frame
    Month 1; Month 6; Month 12; Month18; Month 24
    Title
    Evaluation of the quality of life with the BSHS-B
    Description
    Evaluation of the quality of life of patients by the BSHS-B (Burn Specific Health Scale - Brief). The BSHS-B consists of 40 items divided into four domains with nine subscales (heat sensitivity, affect, hand function, treatment regimens, work, sexuality, interpersonal relationships, simple abilities and body change). Items are answered on a 5-point Likert scale ranging from 0 (extremely) to 4 (not at all).
    Time Frame
    Month 1; Month 6; Month 12; Month 18; Month 24
    Title
    Number of Local side effects
    Description
    wound, device related pain, rash, temporomandibular joint pain, dental pain, suffocating sensation
    Time Frame
    Month 6

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age ≥18 years Post-Burn Face scar during maturation stage or surgical intervention on post-burn face scar during maturation stage Patient agrees to shave beard if necessary for 3D camera measurement Patient able to express informed consent Affiliation to a social security scheme Exclusion Criteria: Post burn face scar in the sequela stage Patient with unbalanced photosensitive epilepsy Patient with an unconsolidated fracture of the face's bones or skull Patient with a known allergy to silicone Pregnant or lactating women
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Nadia OUAMARA, M. Sc, Ing.
    Phone
    03 87 55 77 52
    Email
    n.ouamara@chr-metz-thionville.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Clémence DEFFINIS, MD
    Organizational Affiliation
    CHR Metz Thionville
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Tolerance Assessment of Tailored 3d-printed TFO With Silicone Interface for the Treatment of Post-burn Face Scar

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