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
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
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
NCT ID
NCT04884789
First Posted
February 25, 2021
Last Updated
May 3, 2023
Sponsor
Centre Hospitalier Régional Metz-Thionville
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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