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Vaginal Dryness clinical trials

View clinical trials related to Vaginal Dryness.

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NCT ID: NCT06282614 Not yet recruiting - Vaginal Dryness Clinical Trials

Performance and Safety of MUCOGYNE® Ovule as a Moisturizer

MOVHYDA
Start date: March 2024
Phase: N/A
Study type: Interventional

The aim of this post-Market Clinical Follow-up (PMCF) study is to confirm the efficacy and safety of MUCOGYNE® Ovule in the maintainance of natural moisture of the vulvovaginal mucosa and in the compensation for any natural secretions deficiencies, when used in accordance with its approved labeling, in the context of vulvovaginal dryness.

NCT ID: NCT05156502 Not yet recruiting - Pain Clinical Trials

To Assess Signs and Symptoms in Women Affected by GSM After One Cycle of Pixel CO2-Alma Fractionated Laser

Start date: January 30, 2022
Phase: N/A
Study type: Interventional

Genitourinary syndrome of menopause (GSM) occurs in approximately 50% of menopausal women but is both underrecognized and undertreated despite numerous treatment options. Vaginal dryness, irritation, dyspareunia, urinary frequency, and urinary urgency are some of the more common symptoms that can have a negative effect on women's lives and relationships. In particular, dyspareunia is localized in the vestibule with specific trophic changes more evident than those localized in vagina. The CO2 fractionated laser, has also been found to be useful in several studies for the treatment of vaginal atrophy. In this open comparative study, 70 female menopausal subjects aged between 40 and 70 years old at inclusion, having symptoms of GSM (Vaginal dryness, burning/pain, dyspareunia,dysuria), have given her informed consent and meet all the eligibility criteria, will be enrolled. The two groups of comparison will be 35 subjects treated into vagina and vestibule, versus 35 subjects treated into vagina, only. Subjects will come to a total of 6 visits over a period of 3 months. The primary objective of the study is to evaluate the performance and safety of Pixel CO2-Alma Fractionated Laser comparing its administration into vagina and vestibule versus into vagina, only. The evaluated outcomes are vaginal dryness, burning/pain, dyspareunia, sensitivity to touch at Swab test, Female Sexual Function Index (FSFI) and Vulval Pain Functional Questionnaire (VQ) at day 84 and 120 and the safety during all the study. The secondary objectives are the evaluation of vaginal and vestibular trophism, measured by Vaginal Health Index (VHI) and Vestibular Health Score (VHS) at the FU visits.

NCT ID: NCT03782961 Not yet recruiting - Vaginal Dryness Clinical Trials

Evaluation of Viscosity of a Vaginal Moisturizer

Start date: January 14, 2019
Phase: Phase 4
Study type: Interventional

To evaluate the perception of viscosity of a vaginal moisturizer in postmenopausal women

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: NCT01170195 Not yet recruiting - Clinical trials for Postmenopausal Symptoms

Effectiveness of Licorice Extract Dietary Supplement on the Treatment of Postmenopausal Symptoms

Start date: September 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the proposed study is to test the effect of Licorice Root Extract- Licogen on postmenopausal symptoms in postmenopausal women. Specifically, the study will also test the effect of the licorice extract on vaginal dryness.