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Efficacy of IPL, an Anti-redness Dermocosmetic, and Their Combination in the Treatment of Rosacea

Intense Pulsed Light, a Targeted Anti-Redness Dermocosmetic Regimen, and Their Combination for Erythematotelangiectatic Rosacea: A Comparative Study Using Antera 3D Chromophore Mapping, Grey-Level Co-Occurrence Matrix Texture Analysis and Clinician Erythema Assessment Scale.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07729540
Enrollment
60
Registered
2026-07-27
Start date
2025-09-29
Completion date
2026-04-30
Last updated
2026-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rosacea

Keywords

Erythema, Intense Pulsed Light, Dermocosmetic, Antera 3D Chromophore Mapping, Gray-Level Co-Occurrence Matrix Texture Analysis, Clinician Erythema Assessment, Lumecca, Rosacure

Brief summary

This study compares three approaches to treating persistent facial redness in adults with erythematotelangiectatic rosacea: intense pulsed light (IPL) treatment alone, a professional anti-redness dermocosmetic skincare regimen alone, and the combination of both. The main question the study aims to answer is which of these three strategies is more effective at reducing facial redness, using both clinician grading and objective skin-imaging tools that measure redness and skin texture before and after treatment.

Detailed description

This was a prospective, single-center, three-arm comparative study conducted in an outpatient setting, with 60 adult patients with a dermatologist-confirmed diagnosis of erythematotelangiectatic rosacea allocated to one of three parallel treatment groups (20 patients per group). No randomization or blinding was performed. Group 1 (IPL) received three intense pulsed light treatments with the Lumecca applicator (InMode; 515-1200 nm) at 21-day intervals, with fluence individually titrated to skin response; broad-spectrum SPF 50+ sunscreen was applied after each session, and daily photoprotection was mandatory. Group 2 (dermocosmetic) received four professional in-office anti-redness treatments using the Rosacure Professional system (Synchroline/Cantabria Labs) at 7-day intervals - gentle cleansing, application of Rosacure Professional Serum Booster, and a leave-on regenerating gel mask - together with a standardized 12-week home-care regimen (twice-daily gentle cleanser, Rosacure Intensive SPF 30 in the morning, Rosacure Fast in the evening, and a leave-on mask twice weekly). Group 3 (combination) received the same three IPL treatments as Group 1, immediately followed within the same session by the professional Rosacure protocol, at 21-day intervals, together with the same home-care regimen used in Group 2. Facial redness was assessed using objective imaging (Antera 3D chromophore mapping and Gray-Level Co-occurrence Matrix texture analysis) and by clinician grading, at baseline, 2 weeks after the treatment series, and 8 weeks after the treatment series.

Interventions

DEVICEIntense Pulsed Light (IPL) - Lumecca

IPL treatment (515-1200 nm) delivered with the Lumecca applicator (InMode, Irvine, CA, USA), administered as three sessions at 21-day intervals with fluence individually titrated to skin response.

OTHERRosacure anti-redness dermocosmetic regimen

Professional in-office anti-redness regimen (Rosacure Professional system: gentle cleansing, Rosacure Professional Serum Booster, leave-on regenerating gel mask) plus a standardized 12-week home-care regimen (Rosacure Intensive SPF 30 mornings, Rosacure Fast evenings, leave-on mask twice weekly), manufactured by Synchroline/Cantabria Labs, Spain.

Sponsors

Medical University of Silesia
Lead SponsorOTHER
Synchroline/Cantabria Labs
CollaboratorUNKNOWN

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 57 Years
Healthy volunteers
No

Inclusion criteria

* Adult patients with a dermatologist-confirmed diagnosis of erythematotelangiectatic rosacea

Exclusion criteria

* Age under 18 years * Pregnancy or breastfeeding * Predisposition to keloid or hypertrophic scarring * Use of systemic or topical retinoids, antibiotics, or hormonal therapy within the washout period specified for each agent * Chemical peeling within one month * Laser treatment or phototherapy within three months * Photosensitizing medications or herbal preparations * Inflammatory dermatoses other than rosacea * Autoimmune disease * Active skin infection in the treatment area

Design outcomes

Primary

MeasureTime frameDescription
Antera 3D Erythema Index (Mean, Minimum, and Maximum)Baseline, 2 weeks after the treatment series, and 8 weeks after the treatment seriesErythema quantified via the Antera 3D camera (Miravex, Dublin, Ireland), which reconstructs hemoglobin distribution from multidirectional, multispectral light reflectance and expresses erythema on a reproducible relative scale. For each patient and time point, three erythema indices - mean, minimum, and maximum - were extracted for the left and right cheek and averaged into a single value per index.

Secondary

MeasureTime frameDescription
GLCM ContrastBaseline, 2 weeks after the treatment series, and 8 weeks after the treatment seriesGray-Level Co-occurrence Matrix (GLCM) texture parameter quantifying local brightness variation of the erythematous facial skin from cross-polarized photographs (8-bit grayscale, 256×256 co-occurrence matrix, horizontal offset θ=0°, distance d=1); higher values indicate a more irregular, mottled erythema. Left and right cheek values averaged per patient.
GLCM HomogeneityBaseline, 2 weeks after the treatment series, and 8 weeks after the treatment seriesGray-Level Co-occurrence Matrix (GLCM) texture parameter quantifying surface uniformity of the erythematous facial skin; higher values indicate more uniform erythema. Derived from the same cross-polarized photographs and co-occurrence matrix as GLCM contrast. Left and right cheek values averaged per patient.
Clinician Erythema Assessment (CEA) ScoreBaseline, 2 weeks after the treatment series, and 8 weeks after the treatment seriesSemi-quantitative 5-point ordinal scale (0-4) graded by trained dermatologists, where 0 = no visible erythema and 4 = severe, intense redness; mean of scores from three independent raters.

Countries

Poland

Contacts

PRINCIPAL_INVESTIGATORAnna Deda, PhD

Medical University of Silesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026