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Provoked Localized Vulvodynia clinical trials

View clinical trials related to Provoked Localized Vulvodynia.

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NCT ID: NCT03541512 Enrolling by invitation - Clinical trials for Provoked Localized Vulvodynia

Remote Mindfulness Education PLV

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This is a study designed to learn more about the use of an online remote education and mindfulness practice program for the pain and anxiety associated with provoked localized vulvodynia.

NCT ID: NCT02919813 Completed - Clinical trials for Provoked Localized Vulvodynia

M-gCBT for Women With Provoked Localized Vulvodynia

Start date: December 16, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to learn more about Mindfulness based Group Cognitive Behavior Therapy (M-gCBT) as a treatment for Provoked Localized Vulvodynia (PLV). M-gCBT is a counseling technique that has been shown to reduce pain and anxiety with other medical conditions, including chronic pain conditions. The investigators wish to see if participation in M-gCBT course will help reduce anxiety, fear, and pain in women with PLV greater than education alone. Both techniques use a group setting including other women with PLV. "Mindfulness-Based Group Cognitive Behavior Therapy for Women with Localized Vulvodynia" is a study designed to learn more about the use of mindfulness based group cognitive behavior therapy for PLV pain and anxiety over education alone. Participants will be randomized to one of two groups: mindfulness based cognitive behavior therapy or group education seminars.

NCT ID: NCT02712814 Completed - Clinical trials for Provoked Localized Vulvodynia

Subtypes of Provoked Vestibulodynia

Start date: November 30, 2016
Phase:
Study type: Observational

The proposed study will evaluate a clinical algorithm for the diagnosis and treatment of provoked vestibulodynia (PVD). The algorithm, distinguishes between four subtypes of PVD: hormonally mediated PVD, hypertonic pelvic floor dysfunction, congenital neuroproliferative PVD and acquired neuroproliferative PVD, based on a patient's history and physical exam. The study will follow patients diagnosed with PVD, for one year, and evaluate the treatment outcome in the different subgroups. Investigators hope that conducting a prospective study, showing clinical benefit and improved outcome for patients classified according to this method may change the common practice of "trial and error" based treatment, and will improve clinical results.

NCT ID: NCT01996384 Completed - Vulvodynia Clinical Trials

Provoked, Localized Vulvodynia Treatment With Acupuncture and Lidocaine Pilot Study

Start date: November 2013
Phase: Phase 1
Study type: Interventional

The investigators research project is a randomized, controlled, single-blinded, feasibility pilot study. The investigators will study the feasibility of a novel treatment for women with Provoked Localized Vulvodynia (PLV) with acupuncture and 5% lidocaine cream. Lidocaine is a numbing agent and common first treatment for this disorder. Acupuncture is a treatment commonly used for other pain disorders. The investigators will compare two types of acupuncture (classical and non-classical) as a treatment for PLV, in addition to 5% lidocaine cream. Researchers want to determine if acupuncture is acceptable and convenient to women with PLV. The investigators hypothesize that classical acupuncture and 5% lidocaine cream will be better than non-classical acupuncture and 5% lidocaine cream to decrease PLV pain.