Vaginal Atrophy

11

Review clinical trials related to Vaginal Atrophy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Testing Laser Therapy for Treatment of Vaginal Dryness in Survivors of Breast Cancer, The Revitalize Trial

This phase III trial tests whether vaginal fractional CO2 laser therapy works in treating vaginal dryness in breast cancer survivors. Vaginal dryness can be commonly experienced with normal aging, with menopause, or come about from medications used to treat breast cancer such as chemotherapy or endocrine therapies like tamoxifen or aromatase inhibitors. Vaginal fractional CO2 laser therapy may help reduce vaginal dryness.

Participants needed: 250
Trial details
Phase: Phase 3Age: 22+Biological sex: FemaleType: InterventionalSponsor: Alliance for Clinical Trials in OncologyUpdated: May 11, 2026Locations: 2
Eligibility criteria

Women with a history of breast cancer treated with curative intent who have comp... [+18]

Status: Not yet recruiting

Vaginal Estradiol vs Moisturizer to Improve Postmenopausal Vaginal Aging Symptoms and the Microbiome in Women Living With HIV

This is a research study about the effects of vaginal estradiol compared to moisturizer on vaginal symptoms of menopause and the microbiome in women with HIV. This research study aims to understand how vaginal products affect the aging of the female genital tract in women living with HIV who are menopausal or perimenopausal and have vaginal or urinary symptoms. There is a comparison group of women who are living without HIV. Participants with HIV and vaginal or urinary menopausal symptoms (e.g., dryness, irritation, soreness, itching, pain with sex, dysuria, urgency, or frequent urinary tract infections) will be asked to apply vaginal estradiol or a vaginal moisturizer (Replens). Participants who have vaginal or urinary menopausal symptoms and do not have HIV will receive vaginal estradiol.

Participants needed: 62
Trial details
Phase: Phase 4Age: 40-70Biological sex: FemaleType: InterventionalSponsor: Albert Einstein College of MedicineUpdated: Apr 14, 2026Locations: 1
Eligibility criteria

female [+3]

Unexplained or unevaluated abnormal genital bleeding [+16]

Status: Recruiting

Postpartum Vaginal Estrogen for Breastfeeding Patients

Sexual dysfunction is very common in the postpartum period and is more common in people who breastfeed or pump. This research study was designed to help determine whether postpartum patients who use vaginal estrogen cream while breastfeeding have improved sexual function compared to postpartum patients who do not.

Participants needed: 100
Trial details
Phase: Phase 4Age: 18-50Biological sex: FemaleType: InterventionalSponsor: University Hospitals Cleveland Medical CenterUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Age 18 or older [+7]

Preterm delivery [+4]

Status: Recruiting

VALOR: Vaginal Atrophy & Long-term Observation of Recovery

Vulvovaginal skin conditions, namely vaginal atrophy, lichen sclerosus, lichen simplex chronicus and lichen planus affecting the female adult population will be treated with a novel gel dressing to test the short- and long-term safety and efficacy of the device.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Stratpharma AGUpdated: Feb 20, 2026Locations: 14
Eligibility criteria

Diagnosed atrophic vaginitis, lichen sclerosus, lichen simplex chronicus or lich... [+3]

Unable to provide informed consent [+6]

Status: Recruiting

ASSIST-VLA: Assessment of Symptom-Specific Improvement in Diagnosed Vaginal Atrophy Following Laser Therapy

Vaginal atrophy patients receiving vaginal laser therapy will be treated with daily 7-0940® following a laser session to evaluate the safety and efficacy of the product as an adjunct treatment. Clinical outcomes will be assessed using validated investigator- and patient-reported measures, with safety and symptom progression monitored throughout the study.

Participants needed: 10
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Stratpharma AGUpdated: Jan 16, 2026Locations: 1
Eligibility criteria

Diagnosed vaginal atrophy [+3]

Unable to provide informed consent [+3]

Status: Recruiting

Prevention of Recurrent UTI Using Vaginal Testosterone Versus Placebo Placebo

Women over the age of 60 years have an estimated 10 to 15 % risk of recurrent urinary tract infections (UTI). This is believed to be due to hormonally induced changes in the vaginal flora associated with menopause. After menopause, there is a chemical changes in the vagina that may predispose to bacterial infections. The role of vaginal estrogen creams to restore vaginal atrophy and prevent urinary tract infections has been well characterized. Vaginal testosterone (VT) application use in postmenopausal breast cancer patients on aromatase inhibitors have been shown to improve vaginal pH, vaginal atrophy symptom scores, dyspareunia, and vaginal dryness. Although testosterone has been used to improve sexual function in postmenopausal women, the effects of VT on vaginal flora and recurrent UTIs are unknown. The purpose of this study is to determine whether topically applied vaginal testosterone cream is more effective than placebo in reducing the incidence of urinary tract infections in postmenopausal women with recurrent urinary tract infections and to ascertain the effects of topical estrogen on the vaginal pH and flora.

Participants needed: 100
Trial details
Phase: Phase 4Age: 60-90Biological sex: FemaleType: InterventionalSponsor: Maimonides Medical CenterUpdated: Nov 5, 2025Locations: 1
Eligibility criteria

60-90 yo Female [+7]

Current UTI/ Dipstick and culture positive (> trace leukocytes or nitrites) [+8]

Status: Recruiting

Clinical and Molecular Study to Evaluate the Effect of the Pixel CO2 Laser (FemiLiftTM) for the Treatment of Vulvo-Vaginal Atrophy

Vulvo Vaginal Atrophy (VVA) refers to the changes in the vaginal and vulvar surfaces that occurs during menopause due to the progressive loss of estrogen. The low levels of circulating estrogen produce a wide variety of anatomic, physiologic, and clinical changes in the urogenital area. Clinical symptoms include vaginal dryness, irritation, soreness, dyspareunia, dysuria, and vaginal discharge. In recent years, microablative fractional CO2 laser has become available for treating vaginal atrophy. It showed a regenerative property with significant histological changes in cellular and connective tissue components. Treatment with the fractional CO2 laser resulted in restoration of the vaginal epithelium with ultrastructural findings, similar to a premenopausal state, that included thickened stratified squamous epithelium with increased collagen support, increased glycogen in epithelial cells, increased fibroblasts, increased vascularity, and presence of sub-epithelial papillae.

Participants needed: 20
Trial details
Age: 45-75Biological sex: FemaleType: InterventionalSponsor: Hillel Yaffe Medical CenterUpdated: Jun 17, 2025Locations: 1
Eligibility criteria

Female 45-75 years of age, at the time of enrolment. [+12]

Vaginal Health Index Score (VHIS) < 5. [+17]

Status: Not yet recruiting

Compare Vaginal Estrogen and Platelet-rich Plasma Over Women With Genitourinary Syndrome of Menopause

The definition of Genitourinary Syndrome of Menopause (GSM) is the decline of estrogens during menopause results in symptoms and clinical signs from both systems. Estrogen and other hormones production decrease after menopause because the ovaries lose their effectiveness, leading to mucosal atrophy, reduced vaginal moisture, dysuria, urgency, recurrent infection, burning, pruritus and dyspareunia. The treatment included vaginal estrogen supplement, vaginal hyaluronic acid supplement, vaginal laser, platelet rich plasma, etc. Observational cohort study will be used for study design, and questionnaire, pelvic examination, vaginal pap smear with maturation index (MI), vaginal pH, and other methods will be used for evaluation of the effectiveness and side effects.

Participants needed: 40
Trial details
Age: 45-80Biological sex: FemaleType: ObservationalSponsor: Mackay Memorial HospitalUpdated: May 9, 2025Locations: 1
Eligibility criteria

Women with menopause [+1]

Genitourinary bleeding or infection without definitive diagnosis [+5]

Status: Recruiting

Treatment of Vaginal Atrophy With Low Intensity Nanosecond Neodymium Laser

The aim of study is characteristic of changes in the vaginal wall after treatment of neodymium laser radiation with a wavelength of 1064 nm. To assess the condition of the vaginal walls before and after laser treatment, the following methods will be used: vaginal health index, perineometry, measurement of the vaginal wall thickness by ultrasound, Doppler sonography of the vaginal walls vessels, optical coherence tomography, biopsy, cytological and immunocytochemical methods. The King's Health Questionnaire will be used to collect feedback on changes in the participants life quality. Total up to 100 participants with and 20 participants without postmenopausal atrophy will be involved in the study. Participants will be divided into three groups: laser treatment (study group), topical hormones treatment (control group 1) and no treatment (control group 2) by 70, 30 and 20 participants in each group respectively. The time intervals between special tests and the tests themselves will be the same for all groups. Thus, a direct comparison between conventional treatment (topical hormones), laser treatment of the vaginal atrophy and normal condition without treatment will be made. The main hypothesis of the study is improvement in condition of the vaginal walls after laser treatment compared with the initial state of not less than thirty percent of participants, and improvement in condition on average compared with the control group.

Participants needed: 120
Trial details
Age: 40-75Biological sex: FemaleType: InterventionalSponsor: MeLSyTech, LtdUpdated: Dec 12, 2024Locations: 1
Eligibility criteria

Age of 40-75 years, inclusive; [+2]

Age of under 40 and over 75 years old; [+18]

Status: Not yet recruiting

Hydration and Acceptability of the Genital and Skin Mucosa of a Vaginal Moisturizer in Menopausal Women

Hyaluronic Acid is indicated for the relief of vaginal dryness, itching, and irritation, or the reduction of vaginal lubrication with prolonged hydration effects for up to 72 hours. Hyaluronic Acid promotes vaginal moisture, providing symptom relief in various situations such as: * Vaginismus and other sexual dysfunctions related to penetration * Users of hormonal contraceptives with lubrication loss * Postpartum and lactational period * Post antibacterial or antifungal therapies * During systemic oncological treatments (chemotherapy, radiotherapy, hormone therapy) * Climacteric (urogenital atrophy) * Post urogynecological surgeries (correction of urinary incontinence, genital dystopias, etc.) * Post vulvovaginal abrasive, chemical, laser, or high-frequency therapies * Post cosmetic and genital rejuvenation therapies

Participants needed: 45
Trial details
Phase: Phase 3Biological sex: FemaleType: InterventionalSponsor: Biolab Sanus FarmaceuticaUpdated: Aug 21, 2024
Eligibility criteria

Healthy research participants, with an active sexual life; [+7]

Skin pathology in the area of product application; [+10]

Status: Not yet recruiting

The Efficacy of Topical Vaginal Oxytocin Gel in Postmenopausal Women With Vulvovaginal Atrophy

A Phase three randomized, double-blinded, study to asses the efficacy and safety of oxytocin gel in postmenopausal women with vaginal atrophy due to Genitourinary Syndrome of Menopause GSM.

Participants needed: 244
Trial details
Phase: Phase 3Age: 47-65Biological sex: FemaleType: InterventionalSponsor: OxagonUpdated: Jul 23, 2024Locations: 1
Eligibility criteria

Postmenopausal, sexually active female subject of age 47 - 65 years, at the time... [+1]

Previous treatment with other local non-hormonal moisturizers/hormonal products... [+8]