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Vaginismus clinical trials

View clinical trials related to Vaginismus.

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NCT ID: NCT06397885 Recruiting - Dyspareunia Clinical Trials

Prospective On Market Patient-reported Outcomes for Milli

POMPOM
Start date: April 30, 2024
Phase:
Study type: Observational

To assess the effectiveness of the Milli device in achieving vaginal intercourse

NCT ID: NCT05926752 Recruiting - Pelvic Pain Clinical Trials

Photobiomodulation for Myofascial Pelvic Pain

PMPP
Start date: October 27, 2021
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to evaluate the efficacy of photobiomodulation of the pelvic floor muscles in female Veterans with chronic pelvic pain. The main questions it aims to answer are: - Is there a difference in reduction in overall pelvic pain between women who undergo photobiomodulation compared to women who received pelvic floor physical therapy? - Is there a difference in compliance with therapy between the two groups? Participants will be randomized to treatment with either 9 treatments of photobiomodulation (two treatments per week) or 8 weeks of pelvic floor physical therapy (one treatment a week). Researchers will compare both groups to see if there is a difference in overall pelvic pain reduction.

NCT ID: NCT05529407 Recruiting - Vaginismus Clinical Trials

Trial of SVTampons vs Glass Vaginal Dilators in Treatment of Vaginismus

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the success rates of vaginismus therapy using a tampon or a dilator during exposure

NCT ID: NCT05489133 Recruiting - Clinical trials for Post Traumatic Stress Disorder

Early Psychological Intervention After Rape

EIR
Start date: June 14, 2022
Phase: N/A
Study type: Interventional

Rape is a common cause of post-traumatic stress disorder (PTSD) among women, as around 30-50% will develop PTSD in the aftermath of rape. A modified protocol based on Prolonged Exposure Therapy (mPE), has been developed, consisting of three to five once or twice weekly 60 minutes sessions, and studies indicate that if implemented early after rape, mPE may prevent the development of PTSD. The aim of the study is to conduct a multi-site (4 Sexual assault care centers in Norway) randomized control trial (RCT) in which patients are recruited early after rape, and randomized to intervention (mPE) or treatment as usual (TAU).

NCT ID: NCT04635345 Recruiting - Vaginismus Clinical Trials

Feasibility of Use of Vibrators With Vaginal Dilators for Vaginismus. (Vibrator Therapy and Dilators in Vaginismus)

ViTaDiVa
Start date: August 11, 2021
Phase: N/A
Study type: Interventional

The acceptability of vulvar vibration therapy has been evaluated in women with vulvodynia, and found to be acceptable, however has not been assessed in women with a primary complaint of vaginismus. This proposed study looks at the feasibility and acceptability of using clitoral vibration therapy, alongside current therapy, for women with vaginismus. It is likely that many, if not most, of these women will also have an element of vulvodynia. The investigators propose that the use of external clitoral or vulval vibration therapy is likely to be acceptable in most women with vaginismus, based on acceptability of vulvar vibration therapy in women with vulvodynia. It is proposed that vibrator therapy may help women with female sexual dysfunction to use vaginal dilators.