Evaluation of the Efficacy and Safety of Hyaluronic Acid Injection in Labia Majora for Volume Restoration

Launched by LABORATOIRES VIVACY · Oct 31, 2019

Keywords

ClinConnect Summary

ESOLANE is a prospective multicenter post-marketing study of a class III medical device. This uncontrolled open-label study investigates the efficacy and safety of DESIRIAL® PLUS in volume restoration of Labia Majora. The study duration is 12 months with an optional screening visit (V0) up to 14 days before injection, the baseline visit (injection of DESIRIAL®PLUS, V1) and 5 follow-up visits after 4, 12, 24, 36 and 52 weeks (V2 to V6). At 4 weeks (V2) an optional touch-up may be done (if needed). It is envisaged to enrol 71 female patients with the wish for volume restoration in France to o...

Gender

FEMALE

Eligibility criteria

• Inclusion Criteria:
• Women with the following conditions :
• • ≥ 18 years of age at inclusion
• • Moderate hypotrophy, severe hypotrophy or atrophy of the vulvar Labia Majora, according to the investigator's judgement
• • Expressed the wish for volume restoration of the Labia Majora
• • Able to understand and sign the informed consent for study enrolment
• • Subject affiliated to a health social security system
• • Non-inclusion Criteria
• General :
• • Pregnancy
• • Breast feeding
• • Known tendency to develop hypertrophic scars or keloid scars
• • Participating at the same time in another clinical trial
• • Deprived of their freedom by administrative or legal decision or under guardianship
• Linked to inflammatory or immune status:
• • Known hypersensitivity
• • to one of DESIRIAL® PLUS's components (hyaluronic acid, mannitol)
• • to the antiseptic solution that is planned to be used in this study
• • to amide local anesthetics or to one of the components of the anesthesia product that is planned to be used in this study
• • Presence of clinical signs of inflammatory in or close to the area of interest or treatment for these affections
• • History of or ongoing auto-immune disease
• • Suffering from hemostatic disorder
• Linked to infection:
• • Presence of bacterial, fungal or viral infection in or close to the area of interest or treatment for these affections
• • History of streptococcal illness (such as recurrent sore throat or acute articular rheumatism)
• • Recurrent genital herpes (several times a year)
• Linked to neoplasia:
• • History of cancer in areas close to the injection site (external urogenital, anal or vaginal)
• • Actual cancer or presence of pre-cancerous cells (e.g. vaginal dysplasia)
• Linked to previous or ongoing treatments:
• • Under treatment with aspirin, anticoagulant, platelets aggregation inhibiting drugs, NSAIDs and Vitamin C or treated within 1 week prior to inclusion
• • Under local hyaluronic acid-like hydrating treatment within 4 weeks prior to inclusion
• • History of hyaluronic acid injection of \>14 ml in any part of the body within the last year
• • History of correction with DESIRIAL® range or other resorbable implants with similar indication within 1 year prior to inclusion
• • History of correction with permanent implants including fat graft or semi-permanent in the area of injection
• • Surgical history on Labia Minora within one year prior inclusion
• • Surgical history on Labia Majora