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Completed NCT06661382

Use of Platelet Rich Plasma From Cord Blood vs Placebo in the Treatment of Vulvar Lichen Sclerosus

Conditions: Vulvar Lichen Sclerosus

Sex: Female
Ages: 18 Years – 80 Years
Healthy volunteers: Yes
Phase: PHASE1, PHASE2
Enrollment: 100
Sponsor: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Location: Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico Milan Milan

Summary

Vulvar lichen Sclerosus (VLS) is a cutaneous-mucosal dermatosis that causes in the adult female vulvar itching and burning due to scratching abrasions. Dyspareunia is often associated . The areas most affected are the labia minora, the periclitoral area, the navicular dimple, and the perianal area. The placement of VLS in the context of immune-mediated dermatoses is the basis of the rationale for treatment with high potency topical corticosteroids. However, in some cases, local corticosteroid therapy is not sufficient resulting in a significant impact on the quality of life of the patient. This gives rise to the need to identify new treatments such as regenerative medicine. The term PRP (Platelet Rich Plasma) is used to describe a blood product generated by a two-step centrifugation process of whole blood of a patient to produce a concentration of platelets in a small volume of plasma. PRP can be produced from autologous, homologous blood or from cord blood (CB-PRP). Our objective is to evaluate the efficacy of CB-PRP versus placebo in the treatment of VLS.

Eligibility Criteria

Inclusion Criteria: * women with VLS (clinical/histological diagnosis) * good health conditions * written informed consent signed and dated by the patient Exclusion Criteria: * pregnancy * coagulopathies, platelet disorders, cardiovascular and/or respiratory diseases * ongoing major infections * previous vulvar surgery (e.g., lipostructure and/or previous PRP)

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06661382). StuddyBuddy aggregates publicly available trial information.