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Vaginal Dryness clinical trials

View clinical trials related to Vaginal Dryness.

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NCT ID: NCT03307044 Completed - Breast Carcinoma Clinical Trials

Fractional CO2 Laser Therapy for Survivors of Breast Malignancies

Start date: November 16, 2017
Phase: N/A
Study type: Interventional

This pilot clinical trial studies how well fraction carbon dioxide (CO2) laser therapy works in treating vaginal atrophy in patients with breast cancer. Fraction CO2 laser therapy uses intense beams of light to cut, burn, or destroy tissue and may remodel vaginal tissue and direct controlled thermal damage of vaginal mucosa.

NCT ID: NCT03178825 Completed - Sexual Dysfunction Clinical Trials

Hybrid Fractional Laser for Symptoms of Genitourinary Syndrome of Menopause

Start date: May 19, 2017
Phase: N/A
Study type: Interventional

This multi-center clinical trial will evaluate the safety and long-term efficacy of hybrid fractional 2940 nm and 1470 nm lasers for treatment of symptoms of Genitourinary Syndrome of Menopause.

NCT ID: NCT02994342 Completed - Vaginal Dryness Clinical Trials

Efficacy and Tolerability Study of ZP-025 Vaginal Gel for the Treatment of Vaginal Dryness

Start date: October 2012
Phase: N/A
Study type: Interventional

Evaluation of ZP-025 vaginal gel in terms of efficacy and safety in the treatment of vaginal dryness in post-menopausal women with vaginal atrophy in comparison to a group of non-treated post-menopausal women with vaginal atrophy after 56 consecutive days and at 4-week follow-up only for women applying ZP-025 vaginal gel.

NCT ID: NCT02987647 Not yet recruiting - Vaginal Dryness Clinical Trials

Perception of Efficacy, Safety and Tolerability of Three Non-hormonal Intravaginal Gels and Hormone Cream

Start date: January 2017
Phase: Phase 4
Study type: Interventional

To evaluate the perception of the effectiveness of Hidrafemme® gels, Vagidrat®, Lubrinat and Antrofi cream in improving vaginal moisture in postmenopausal women who are currently registered options most current and available in the market in order to assess the differences between them, subsequently conduct a clinical study larger.

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.

NCT ID: NCT02638337 Completed - Vaginal Dryness Clinical Trials

Study to Evaluate Ospemifene in Patients With Moderate to Severe Vaginal Dryness Due to Menopause

Start date: January 26, 2016
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of ospemifene 60 mg once daily (QD) compared with placebo in treatment of vulvo-vaginal atrophy (VVA) due to menopause in women with moderate to severe vaginal dryness as the most bothersome symptom (MBS) of VVA.

NCT ID: NCT02269826 Completed - Vaginal Dryness Clinical Trials

Efficacy and Safety of Non-hormonal Vaginal Preparations in Treating Vaginal Dryness

Start date: February 2008
Phase: N/A
Study type: Interventional

Vulvovaginal irritation due to dryness is a frequent complaint among post- and some premenopausal women. International guidelines recommend non-hormonal products as first line therapy. Efficacy and safety of the medical device Vagisan® Moisturising Cream (VMC), a non-hormonal vaginal cream for the treatment of vulvovaginal dryness and Gynomunal Vaginal Gel (GVG), a non-hormonal gel should be compared in a 12-week multicentre, open-label, randomised, two-period cross-over phase III trial. The hypothesis was that VMC is non-inferior to GVG. The primary endpoint was the sum of subjective symptoms of vulvovaginal atrophy (VVA) added up over each treatment period. Furthermore, objective symptoms of VVA and adverse effects were planned to be assessed. 120 women should be randomly allocated to either of the two treatments, each given over a period of 4 weeks.

NCT ID: NCT02176083 Completed - Breast Cancer Clinical Trials

Reproductive Health Survivorship Care Plan Pilot

Start date: March 20, 2014
Phase: N/A
Study type: Interventional

Most young breast cancer patients undergo chemotherapy and/or endocrine therapy, treatments that impair ovarian function and result in significant reproductive health late effects. These late effects include symptoms of estrogen deprivation (e.g., hot flashes and vaginal dryness), which are distressing in young breast cancer survivors (YBCS). The goal of this pilot study is to test the feasibility of a 4-week text message based intervention on hot flashes and vaginal dryness in YBCS. YBCS will be randomized in a 1:1 ratio to the intervention (text messages on hot flash and vaginal dryness management) and control arms. All participants will be prompted to provide daily hot flash frequency and severity via text messaging. The primary hypothesis is YBCS will have high rates of daily hot flash reporting via text messaging. Secondarily, we will compare changes in hot flash frequency, hot flash severity and vagina dryness between the intervention and control arms.

NCT ID: NCT01948583 Completed - Menopause Clinical Trials

Humectant Activity of a New Formulation of Gynomunal® Vaginalgel

GYNOMUNAL®
Start date: May 2013
Phase: Phase 4
Study type: Interventional

Aim of the study is to evaluate the humectant activity and the local tolerability of a new formulation of Gynomunal® vaginalgel in menopausal women (menopause since at least 2 years) with referred vaginal dryness

NCT ID: NCT01724242 Withdrawn - Breast Cancer Clinical Trials

Vaginal DHEA for Women After Breast Cancer

Start date: February 2013
Phase: Phase 2/Phase 3
Study type: Interventional

There does not appear to be a consensus regarding the treatment of vaginal dryness in women who have a contraindication to the use of estrogen products. DHEA, when used locally, may improve the symptoms of vaginal dryness due to its chemical properties.