We pride ourselves to be the very first leading clinic to introduce the revolutionary dermal fillers - Ellanse from Holland into the UK, by Dr Ayham Al-Ayoubi in March 2010.
Ellanse developed by AQTIS Medica, is the first dermal filler which offers a safe unique Tunable Longevity specifically designed for the field of aesthetic medicine and surgery with the result lasting from 3-5 years.
Ellanse is made of Poly-caprolactone (PCl), is a well-known totally bioresorbable soft medical polymer. PCl is used in numerous CE-marked and Food and Drug Administration (FDA) approved commercial bloresorbable product applications for several decades world-wide and has demonstrated an excellent safety profile.
ELLANSE offers the maximum potential for modeling due to the combination of optimum viscosity, unique elasticity and uniform homogeneity. Hence, the ELLANSE Family can be used in a variety of beautifying indications:
The ELLANSE is an injectable implant, indicated for deep dermal and subdermal implantation. The nasolabial folds used in the clinical study are representative for deep and sub-dermal soft tissue augmentat ion of the facial area.
With the unique elasticity and optimum viscosity, ELLANSE provides the additional advantage of targeted placement. Thereby allowing cost-effective correction of facial wrinkles and folds.
The excellent performance and saftey of the Ellanse is well grounded in its mode of action and specificaly tunable characteristics.
The technology of AQTIS Medical has been developed from a design and performance perspective to optimze the safety profile of the Ellanse. The unique totally smooth ans spherical shape of the Ellanse microspheres is the basis fror optimal biocompatibily. This as rough surfaces and irregular shaped microparticles have a greater propensity to induce adverse events and result in decreased collagen deposition.
The specifically designed microsphere characteristics provide a safe and long-lasting high quality scaffold for tissue infiltration.
The ong-term safety and total bioresorption of Ellanse components through the normal metabolic pathways has been well documented by numerous scientific biocompatibility studies and literature research. For the PCL-microspheres this has additionally been demonstrated via radio-labeled bioresorption studies. Totally bioresorbable dermal fillers guarantee the absence of long-term side effects and give you the benefit of reversible results.
Patient satisfaction at 12 months evaluated on the basis of GAIS (Global Aesthetic Improvement Scale) for Ellanse was found to be 90%. Average physician evaluation shows improvement in 92% patients based on GAIS.
Ellanse treatments were rated to be EXCELLENT or GOOD by 97% patients on the scale of likelihood to return for repeat treatment at 12 months.
The unique advantages of ELLANSE are Sustained Performance, Tunable Longevity and Total Bioresorbability.
The optimum combination of high viscosity and unique elasticity distinguishes it from the more fluid and short-lasting HA-fillers In addition, ELLANSE stimulates the generation of new collagen tissue unlike HA-fillers, which are volumizers.
No. ELLANSE is a non-animal, non-bacterial and non-human derived product.
Very few have been reported in the clinical trial. However, common and expected injection-related side effects like swelling, redness and bruising might occur.
![]() By Dr Ayham Al-Ayoubi Before |
![]() By Dr Ayham Al-Ayoubi After |
Ellanse
Ask Dr Ayoubi