Keloid
Conditions
Keywords
Keloid, Dermatology, Bleomycin, Jet-injection
Brief summary
This is a single center, double-blind (patient and investigator), randomized, placebo-controlled study with a split-lesion design, in which selected keloids will receive three consecutive treatments of a) bleomycin and b) placebo (saline (NaCl 0,9%)), administered with an electronic pneumatic jet injector.
Detailed description
This is a single center, double-blind (patient and investigator), randomized, placebo-controlled study with a split-lesion design.All study procedures will be performed at the Department of Dermatology, Erasmus MC Medical Center in patients referred for scar treatment to our outpatient clinic. Clinical photos will be obtained after signing the informed consent form by patient and investigator. Study visits and clinical assessments will be scheduled at baseline, 4 weeks, 8 weeks, and 12 weeks. Measurements include clinical photography, scar volume measured by 3D-camera, POSAS questionnaire, laser speckle contrast imaging to visualize keloid scar vascularization, measurement of residue formation on the skin, and a treatment related questionnaire. The keloid will be divided into two treatment areas, and randomly assigned to three consecutive treatments of: a) bleomycin and b) placebo (saline (NaCl 0,9%)), administered with an electronic pneumatic jet injector.
Interventions
DRUGBleomycin
Intralesional bleomycin treatment administered with an electronic pneumatic jet injector
DRUGNormal saline
Intralesional placebo treatment of normal saline administered with an electronic pneumatic jet injector
Sponsors
Centre for Human Drug Research, Netherlands
Erasmus Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Intervention model description
A single center, double-blind (patient and investigator), randomized, placebo-controlled study with a split-lesion design.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Subject has provided written informed consent; 2. Subject is ≥ 18 years of age at time of screening; 3. Subject has at least one keloid scar of ≥ 4 cm in length, or two separate keloids with a length of ≥2cm, with a minimum \> 1.0 cm apart in the same anatomical region. 4. Subject is willing to fill in questionnaires and take photos using an e-diary application on their phone.
Exclusion criteria
1. Known hypersensitivity to any component of the test materials; 2. Pregnant or breast-feeding women (pregnancy test prior to treatment); 3. Previous bleomycin treatment of the keloid within the last 12 weeks prior to screening. 4. Non-response to previous bleomycin treatments of the keloid. 5. Any medical or psychiatric condition which, in the investigator's opinion, would preclude the participant from adhering to the protocol or completing the study per protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Volume reduction | 12 weeks | Volume reduction of scar tissue in mm\^3. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Vascular perfusion | 12 weeks | Evaluation of changes in keloid vascular perfusion using Laser Speckle Contrast Imaging. |
| Residue formation on skin | 30 minutes | Evaluation of the average residue formation on skin in percentage of the injection volume. |
| Procedure related pain | 30 minutes | Evaluation of the procedure related pain using a numerical rating scale (NRS) score. This scale ranges from 0-10 points, with higher scores indicating greater pain intensity. |
| Clinical efficacy using Patient and Observer Scar Assessment Scale (POSAS) | 12 weeks | Evaluation of clinical efficacy using Patient and Observer Scar Assessment Scale. The POSAS consists of six items (vascularization, pigmentation, thickness, relief, pliability and surface). Each item will be scored on a scale from 1 (normal skin) to 10 (worst scar). The scores of these six items result in the 'POSAS total score', also on a scale from 1 (normal skin) to 10 (worst scar). |
| Treatment satisfaction | 12 weeks | Evaluation of treatment satisfaction using a 5-point Likert scale. This scale ranges from -2 to 2 points, with higher scores indicating higher satisfaction. |
| Incidence of Treatment-Emergent Adverse events [Safety and Tolerability]. | 12 weeks | Evaluation of safety and tolerability by evaluating all adverse events. Patients will daily be asked to take pictures of the treated lesion(s), and to report any adverse event via an digital e-diary application. |
| Local skin reactions | 12 weeks | Evaluation of the local skin reactions using self-taken photos in an e-diary. |
Countries
Netherlands
Outcome results
None listed