Expected reduction of 25% on the DQOL score.
ID
Bron
Verkorte titel
Aandoening
Vulvar Lichen Sclerosus
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Efficacy is determined by the quantification of improvement in patient’s symptoms by improvement in quality-of-life and sexual functioning three months, six months and one year after injection of SVF enriched lipoaspirate. Quality of life is evaluated using the validated Dermatology Life Quality Index (DLQI) and resumption of sexual activity and quality of sexual functioning is evaluated using the validated Female Sexual Function Index (FSFI).
Achtergrond van het onderzoek
Lichen sclerosis (LS) is a chronic inflammatory dermatosis with a high prevalence in the genital area in peri- or postmenopausal women. Vulvar LS presents with progressive pruritus and pain, sexual and urinary dysfunction, reduced quality of life, and an increased risk of vulvar squamous cell carcinoma. In patients treated for vulvar cancer, the presence of LS appears to affect the incidence of recurrence of squamous cell carcinoma.
Transfer of adipose tissue, also known as lipofilling, is recognized as a promising and novel technique for the treatment of a range of pathologies. The white adipose tissue harbors a mesenchymal cell population with stem cell-like properties, which holds regenerative potential.
The aim of the study is to evaluate the safety and efficacy of lipofilling with additional SVF-enriched lipoaspirate for the treatment of vulvar LS in non-responders to conventional treatment. Efficacy is determined by the quantification of improvement in patient’s symptoms by improvement in quality-of-life and, if applicable, in sexual functioning. Secondary objectives are the quantification of improvement in clinical signs by physical examination findings and improvement of histopathological parameters. In addition the molecular mechanism of regeneration of sclerosis is evaluated
Doel van het onderzoek
Expected reduction of 25% on the DQOL score.
Onderzoeksopzet
3,6 and 12 months
Onderzoeksproduct en/of interventie
Pilot study to evaluate the safety and efficacy of vulvar injection of SVF enriched lipoaspirate in women with therapy-resistant vulvar LS.
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
• Postmenopausal women up to 80 years with ASA Physical Status Classification 0-1
• Histopathological confirmed diagnosis of lichen sclerosus
• Moderate or severe LS (IGA scale 3 or 4), therapy resistant to conventional therapy with highly potent topical steroids
(insufficient reduction in clinical symptoms and signs having used topical steroids for 6 months).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
• Women with history of vulvar cancer or VIN in addition to lichen sclerosus.
• An oncological event in the patient’s history < 5 years ago.
• A known systemic disease that will impair wound healing (e.g. diabetes mellitus type I, known atherosclerosis with an event
that required hospitalization, collagen diseases, diseases of the skin, HIV).
• Systematic use of prednisone or other immunotherapy.
• Use of anticoagulant therapy.
• Smoking.
Opzet
Deelname
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In overige registers
| Register | ID |
|---|---|
| NTR-new | NL7908 |
| CCMO | NL65403.000.18 |
| OMON | NL-OMON48736 |