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Vulvar Pain clinical trials

View clinical trials related to Vulvar Pain.

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NCT ID: NCT05478746 Completed - Vulvodynia Clinical Trials

Effects of Flourish HEC on Localized Provoked Vulvodynia

Start date: September 26, 2022
Phase: N/A
Study type: Interventional

This study is designed to determine whether improving the vaginal microbiome in women with localized provoked vulvodynia (LPV) may help improve pain better than routine care alone. The study randomizes women with LPV to either routine care or routine care plus a vaginal hygiene system designed to improve the vaginal microbiome. Women will be assessed for vaginal microbiome, vaginal pH, and pain before enrollment and after 6 weeks, and after 3 months. Women will also have pain assessed 2 weeks after enrollment without assessing vaginal microbiome and pH.

NCT ID: NCT05343182 Recruiting - Vulvodynia Clinical Trials

Vestibulectomy Surgical Techniques Comparison Study

Start date: October 6, 2022
Phase: N/A
Study type: Interventional

Vestibulectomy Surgical Techniques Comparison Study

NCT ID: NCT04016467 Terminated - Vulvodynia Clinical Trials

Effect of Spinal Manipulation on Vulvar Pain

SpManipPP
Start date: May 10, 2019
Phase: N/A
Study type: Interventional

The purpose of the study is to determine the effect of thoracic spine manipulation on vestibule pain as determined by sensory testing (q-tip and pressure algometry) in a group of women with provoked vestibulodynia (PVD). The objective is to compare the immediate effect of manipulation and sham manipulation on the results of sensory testing of the external vulva, or vestibule.

NCT ID: NCT03481621 Recruiting - Vulvodynia Clinical Trials

Effect of Two Acupuncture Protocols on Vulvodynia

Acu/Vul-pain
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

Vulvodynia is a common condition in women (16%); however, at this time there is no known effective non-pharmacological therapy reported. Acupuncture is one complementary and alternative medicine therapy used by many patients with vulvodynia; some case reports show that acupuncture may be an effective intervention. In recent years, there were some studies registered took at like at actual trials of acupuncture on vulvodynia, but either they did not reach the trial aims, some studies did not get enough patients or the trial designs mimic drug studies and did not reflect acupuncture real characteristics. This study evaluates acupuncture for the treatment of vulvodynia; specifically, if it reduces vulvar pain, pain duration and pain with intercourse. It also examines how long the effect of acupuncture lasts in women with vulvodynia. One third of the women will receive acupuncture focused on pudendal nerve distribution area; another one third of the women will receive acupuncture focused on traditional meridian points; the other one third of women will use standard care (without acupuncture). Women who get a reduction in pain (included in subjective and objective scores) will have their pain monitored once a week for up to 6 weeks to see if the acupuncture effect lasts.

NCT ID: NCT00496184 Completed - Vulvodynia Clinical Trials

Efficacy Study of Topical Application of Nifedipine Cream to Treat Vulvar Vestibulitis

Start date: April 2006
Phase: Phase 3
Study type: Interventional

To evaluate the use of topical application of Nifedipine cream for the treatment of Provoked localized Vulvodynia (vestibulitis, vestibulodynia).