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Vaginal Atrophy clinical trials

View clinical trials related to Vaginal Atrophy.

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NCT ID: NCT06391372 Not yet recruiting - Menopause Clinical Trials

Effect of Local Estriol Treatment Before Vaginal Repair Surgery

Start date: April 2024
Phase: Phase 3
Study type: Interventional

The aim of the study is to evaluate the effects of local estriol treatment applied before vaginal repair surgery on steroid receptors, inflammatory cell response, vascular, connective and nervous tissues in the vagina, and its effects on early postoperative period pelvic floor functions, satisfaction with the surgery and vaginal health.

NCT ID: NCT06353945 Not yet recruiting - Vaginal Atrophy Clinical Trials

Perceived Effectiveness of the Vaginal Moisturizer Investigational Product Under Normal Conditions of Use.

Start date: April 29, 2024
Phase: N/A
Study type: Interventional

The present research project aims to evaluate the perceived effectiveness of the product under investigation under normal conditions of use for 28 days, to defend the claims "High hydration power, relief of discomfort and improvement of vaginal tone."

NCT ID: NCT05483634 Not yet recruiting - Menopause Clinical Trials

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

Start date: October 28, 2022
Phase:
Study type: Observational

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.

NCT ID: NCT05457972 Not yet recruiting - Breastfeeding Clinical Trials

Postpartum Vaginal Estrogen for Breastfeeding Patients

Start date: July 1, 2024
Phase: Phase 4
Study type: Interventional

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.

NCT ID: NCT05379153 Not yet recruiting - Clinical trials for Anatomic Stage III Breast Cancer AJCC v8

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

Start date: December 2024
Phase: Phase 3
Study type: Interventional

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.

NCT ID: NCT03238053 Not yet recruiting - Breast Cancer Clinical Trials

Laser Treatment of Genito-urinary Syndrome in Women

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

Women with genitourinary syndrome of menopause, overactive bladder, with breast or endometrial cancer are randomized to either laser treatment og sham treatment for 3 months. The randomization is stratified for estrogen treatment. The effect is evaluated by questionnaire, histology and microbiology swaps

NCT ID: NCT02571127 Not yet recruiting - Vaginal Atrophy Clinical Trials

Evaluate the Efficacy, Safety and Tolerability of a Non-hormonal Intravaginal Gel in Postmenopausal Women With Symptoms of Vaginal Dryness.

Start date: October 2015
Phase: Phase 4
Study type: Interventional

Primary: Evaluation of improved vaginal moisture in postmenopausal women. Secondary: the improvement of symptoms resulting from the dryness Rating (VHI), evaluation of the decrease in vaginal pH, assessment of Sexual Function Index female (FSFI), evaluation of adherence to study treatment by patient diary, assessing the acceptability of the product and subjective assessment of the patient as the itching and stinging / burning, beyond the safety assessment.

NCT ID: NCT00453089 Not yet recruiting - Vaginal Atrophy Clinical Trials

VG101 Phase I/II to Treat Vulvar and Vaginal Atrophy in Post-Menopausal Women

Start date: June 2012
Phase: Phase 1/Phase 2
Study type: Interventional

To conduct a prospective, randomized, blinded, placebo controlled, dose escalation clinical trial in 4 cohorts of 10 postmenopausal women (total N=40) aged 45 to 65 years with at least one menopausal vaginal symptom, vaginal pH > 5.0 and > 20% parabasal vaginal epithelial cells.