CLINICAL SCULPT | UPPER BODY
$250.00
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YOUR CART IS STILL HERE Items on sale, but not for long!
YOUR CART IS STILL HERE Items on sale, but not for long!
Sculpting action that improves contour and the appearance of stubborn fat, with visible results on the upper body in just 15 days.
Body treatment by application with LipoActive™, the Biomimetic Complex that activates your body.
Most awarded brand 
Independent Proven Results 
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THE COSMETIC ALTERNATIVE TO INVASIVE PROCEDURES.
Reduce. Redefine. Resculpt.
A body sculpting treatment by application that targets stubborn fat and the areas that just don't respond.
Formulated with LipoActive™, a biomimetic sculpting complex exclusive to COCUNAT that activates natural skin processes linked to improving stubborn volume and body contour; we Reactivate, Reduce and Redefine localised volume.
Designed to act exactly where the body stops responding, working precisely on the most resistant areas.
Independent clinical results*. Helps you reduce up to:
• -11 cm on abdomen*
• -5 cm on arm*
• 34% improvement in cellulite*
*Result of an independent clinical test, over 45 days, 3 applications, on 19 volunteers, using optimized application. The reduction is proportional to the volume to be reduced.
Designed to be easy. Tested to deliver results. Backed by science.
The efficacy of this treatment is backed by rigorous clinical tests carried out in independent laboratories on 19 female volunteers and verified through mechanical and instrumental measurements.
Full body treatment (after three applications) 45 days:
Helps reduce UP TO:
• -11 cm on abdomen
• -5 cm on arms
• Visible cellulite improvement of 34%
1 body application (after a single 15-day application):
Helps reduce UP TO:
• 7.6 cm on abdomen
• 3.3 cm on arms
CLINICAL TEST OBJECTIVE
To evaluate the reducing, firming, and toning efficacy of CLINICAL SCULPT in areas with localized fat and/or visible cellulite, in healthy adult women, over 6 weeks and after 3 controlled applications of the product.
The product's efficacy was evaluated in an independent clinical study conducted under medical supervision, analyzing its effect on:
• Improving skin firmness and elasticity
• Visibly reducing the appearance of cellulite
• Improving the appearance of body contour
• Reducing circumference in different treated areas
The evaluated areas were: abdomen, arms, thighs, and double chin.
The study was conducted on women aged 25 to 65 with the presence of cellulite and/or skin sagging, following controlled advanced application conditions and standardized instrumental protocols.
Clinical methodology and quality assurance
Evaluating the efficacy of cosmetic products requires a multidimensional approach that integrates various methodologies and tools. To ensure precise and reliable results, clinical and technological instruments are used to allow an objective and quantitative evaluation of skin parameters. These instruments have been selected for their ability to measure critical aspects such as firmness, elasticity, clinical evaluation of cellulite, and circumference reduction in localized areas. The combination of these methods provides solid data supporting the product's efficacy and safety claims.
The clinical study was conducted by a laboratory specialized in clinical evaluation and instrumental studies applied to cosmetics and dermatology.
The evaluations were carried out under medical supervision, under controlled clinical conditions, and following Good Clinical Practice (GCP) protocols, guaranteeing the objectivity, precision, and reproducibility of the results obtained.
Quality and standards applied in the study
• Studies conducted in accordance with Good Clinical Practice (GCP) protocols
• Validation of experimental protocols by an Independent Ethics Committee
• Instrumental and clinical evaluations performed by specialized personnel
• Reports developed under criteria of scientific rigor, objectivity, and methodological control
• Possibility of monitoring and auditing clinical studies
• Studies backed by ISO 9001:2015 certified laboratories
• Specialized scientific-technical and toxicological advisory
CLINICAL TEST RESULTS
EVALUATION OF THE REDUCING EFFECT
Measurements were performed in a controlled clinical environment, under medical supervision, and using specialized instrumentation to guarantee the objectivity, precision, and reliability of the results.
The reducing effect was evaluated through the objective measurement of body circumferences in the different treated areas.
The clinical results showed visible and measurable reductions from the first application, with progressive improvements after 3 applications.
Results after 1 application
ABDOMEN
• average circumference reduction of 0.50 cm*
• maximum observed reduction of up to 7.6 cm
• visible improvement in circumference in 45% of volunteers
*p-value=0.4399
ARMS
• average circumference reduction of 1.12 cm*
• maximum observed reduction of up to 3.3 cm
• visible improvement in circumference in 70% of volunteers
*p-value=0.0026
Results after 3 applications
ABDOMEN
• average circumference reduction of 2.70 cm*
• maximum observed reduction of up to 11 cm
• visible improvement in circumference in 63% of volunteers
*p-value=0.0223
ARMS
• average circumference reduction of 1.58 cm
• maximum observed reduction of up to 5 cm
• visible improvement in circumference in 74% of volunteers
*p-value=0.0009
EVALUATION OF SKIN FIRMNESS AND TONICITY
Skin firmness and elasticity were evaluated using Cutometer® biometric technology, an instrument used in dermatological research to objectively measure mechanical resistance and skin recovery capacity.
The evaluations were performed under controlled clinical conditions, under medical supervision, and through specialized instrumental methodology.
Results after 1 application
ABDOMEN
• 50% improvement in skin firmness
• p<0.0001 - statistically significant improvement in the skin's mechanical resilience
ARMS
• 31% improvement in skin firmness
• p<0.0001 - statistically significant improvement in the skin's elastic behavior
Results after 3 applications
ABDOMEN
• 54% improvement in skin firmness
• p<0.0001 - statistically significant improvement in skin elasticity and mechanical resistance
ARMS
• 52% improvement in skin firmness
• p<0.0001 - statistically significant improvement in skin elasticity and tonicity
The results showed less skin deformation in response to mechanical stimuli, a clinical indicator associated with firmer, more toned, and resilient skin.
CLINICAL EVALUATION OF CELLULITE
Cellulite is one of the most frequent aesthetic alterations in women's skin and visibly affects skin texture and uniformity. Due to its multifactorial nature, its evaluation requires standardized clinical methodologies to objectively measure visible changes in the skin over time.
For this study, the Nürnberger-Müller clinical scale was used, a dermatological methodology widely used to classify the grade of cellulite and evaluate its evolution following treatment. This scale allows a standardized assessment of visible parameters such as skin relief, the "orange peel" appearance, and skin surface irregularity, both at rest and through manual compression.
The use of this clinical methodology, alongside the evaluations conducted under medical supervision, allowed an objective analysis of the visible improvement in cellulite-prone skin after successive applications of the product.
Results after 3 applications
ABDOMEN
• 52% clinical improvement in the appearance of cellulite evaluated using the Nürnberger-Müller dermatological scale*
• visible improvement in 74% of volunteers
• clinically highly significant improvement
*p-value=0.0007
ARMS
• 41% clinical improvement in the appearance of cellulite evaluated using the Nürnberger-Müller dermatological scale
• visible improvement in 58% of volunteers
• clinically highly significant improvement
*p-value=0.001
OBSERVED CLINICAL RESULTS
Clinical evaluations confirmed:
• visible improvement in the appearance of cellulite-prone skin
• decrease in skin irregularities
• improvement in the "orange peel" appearance
• progressive improvement of skin relief after successive applications
Results obtained under medical supervision using a standardized clinical methodology of dermatological evaluation.
TEST TIMING & OPERATION
The clinical study had a total duration of 6 weeks, and 3 controlled applications were performed, spaced every 14 days.
To objectively evaluate the efficacy of the product, validated instrumental and clinical methodologies were used, and statistical significance was considered for p-values < 0.05.
BIOMECHANICAL EVALUATION OF FIRMNESS AND ELASTICITY
Measurements were performed using a Cutometer™ (Courage + Khazaka electronic), a technology used in dermatological research to analyze:
• Skin firmness
• Elasticity
• Skin recovery capacity
• Mechanical resistance of the tissue
The device measures how the skin responds to a controlled micro-aspiration, allowing objective quantification of changes in tonicity and elasticity.
CLINICAL EVALUATION OF CELLULITE
Cellulite was evaluated using the Nürnberger-Müller clinical scale, a recognized dermatological methodology to visually classify the grade of cellulite and detect relevant clinical improvements throughout the treatment.
EVALUATION OF THE REDUCING EFFECT
Body circumference measurements were performed in all treated areas to objectively quantify the reducing effect of the treatment.
SAFETY AND TOLERABILITY
The study was conducted under medical supervision and dermatological control, recording tolerability, potential skin reactions, and subjective perception of efficacy by the volunteers through final questionnaires.
Designed to be easy. Tested to deliver results. Backed by science.
3 APPLICATIONS (1 every 15 days).
The upper body treatment covers two areas: the abdomen (front and sides) and the arms. Each area has its own application pattern.
1. Prep your skin
Wash your hands and clean the application area with soap or micellar water.
2. Apply the pulses
• Abdomen and Arms: Apply 15 pulses on each area following the dot pattern.
• Abdomen sides: Apply 8 pulses in total on each side following the dot pattern.
3. Massage until absorbed
Once you've applied the full serum, massage gently until fully absorbed.
For external topical use only. Avoid eyes, eyelids, lips and mucous membranes. Keep out of reach of children.
Microneedling tools
To boost the efficacy of the treatment, combine it with microneedling tools such as a dermaroller or other microstimulation systems.
This type of application creates microchannels in the skin that allow much deeper and more even absorption of the actives, maximising their impact.
Scan the QR code and discover how to adapt the application depending on the tool to get visible results from the very first applications.
Elevate your routine
Pair and boost your results with BODY POWER, the cellulite-reducing body gel.
• Morning and/or evening: Apply SMART BURN to the target areas (abdomen, thighs, hips, arms) and massage with circular movements until fully absorbed.
• Before physical activity (even walking or dancing): Apply WARM UP to the target area, massaging actively until absorbed.
After applying CLINICAL SCULPT, wait 24/48 hours before applying BODY POWER.
A combination of a biomimetic sculpting complex exclusive to COCUNAT plus advanced actives that work directly on stubborn fat to help you reduce volume, improve skin texture and redefine body contour in a TRULY EFFECTIVE way.
CLINICAL SCULPT | UPPER BODY