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Vulvar Atrophy clinical trials

View clinical trials related to Vulvar Atrophy.

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NCT ID: NCT05378269 Completed - Vulvar Atrophy Clinical Trials

Study of Intravaginal Tamoxifen in PostMenopausal Women With VVA

DARE-VVA1
Start date: November 22, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the study is to study the safety, PK and PD of Intravaginal Tamoxifen on postmenopausal women with vulvar vaginal atrophy.

NCT ID: NCT04705883 Completed - Breast Cancer Clinical Trials

Vaginal Prasterone In Vaginal Atrophy In Breast Cancer Survivors

VIBRA
Start date: September 1, 2020
Phase: Phase 4
Study type: Interventional

VAGINAL PRASTERONE in the treatment of VAGINAL ATROPHY IN PATIENTS WITH BREAST CANCER TREATMENT WITH AROMATASE INHIBITORS (VIBRA STUDY)

NCT ID: NCT04147689 Completed - Vulvar Atrophy Clinical Trials

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

ESOLANE
Start date: November 18, 2019
Phase: N/A
Study type: Interventional

DESIRIAL® PLUS is a CE-marketed hyaluronic acid (since 2011) whose registered indications are moderate hypotrophy, severe hypotrophy or atrophy of the vulvar Labia Majora by subcutaneous injections. The aim is to restore volume, rehydrate and add tone and tension to connective tissue areas by filling. In this study, 71 female subjects above or equal to 18 years old at inclusion, who have moderate hypotrophy or severe hypotrophy or atrophy of the vulvar Labia Majora (according to investigator's judgement), who have given her informed consent and meet all the eligibility criteria, will be enrolled. Subjects will come to a total of 6 visits over a period of 12 months. An optional screening visit may be done before injection (additional visit). Proportion of patients having an improved perception of aesthetics (GAIS score after mirror self-examination) after baseline injection will be assessed. Global Aesthetic Improvement, Sexual function, subject's satisfaction, subject's symptoms, pain at injection and safety will be also assessed.

NCT ID: NCT02966925 Completed - Vulvar Atrophy Clinical Trials

Autologous Platelet Concentrate Combined to Hyaluronic Acid Obtained With Cellular Matrix® BCT-HA Kit and Vulvovaginal Dryness

Start date: March 2016
Phase: N/A
Study type: Interventional

Vulvovaginal irritation is a frequent complaint among postmenopausal women. Common symptoms of vaginal atrophy include dryness, itching, burning and dyspareunia. This pilot study will assess the efficacy of platelet-rich plasma (PRP) combined to hyaluronic acid (HA) to relieve vulvovaginal dryness in patients who cannot benefit from reference treatments (hormonal therapies).To achieve this, 20 patients suffering from vulvovaginal dryness will be treated with one session of injections in the vulva, the posterior vaginal wall and the perineum, and followed-up for 6 months. Improvement of vaginal dryness will be primarily appreciated through Friedmann score and pH value, and secondarily through the Female Sexual Function Index (FSFI), as measured at baseline and 1, 3 and 6 months after the treatment.

NCT ID: NCT02937805 Completed - Vaginal Atrophy Clinical Trials

Effects of a Moisturizing Cream on Vaginal and Vulvar Mucous Membranes

Start date: October 2016
Phase: N/A
Study type: Interventional

Vulvovaginal atrophy is a common problem associated with decreased levels of estrogen. Typical symptoms include feelings of dryness and uncomfort of the mucous membranes of intimate area. The objective of this study is to investigate the effects of a non-hormonal moisturizing cream on symptoms and signs of vulvovaginal atrophy and dryness.