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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.

NCT ID: NCT04436172 Completed - Vaginismus Clinical Trials

Spinal Anesthesia Facilitated Sexual Intercourse As A Treatment Option For Vaginismus

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Painful sex continues to be a relationship issue and can lead to marital dys-harmony. Other consequences include infertility, low self-esteem, depression and anxiety.Our study shows that spinal anesthesia is an effective last resort management option in women with vaginismus. As a one-off treatment spinal anesthesia provides hope for such couples and brings about a positive change in their relationships.

NCT ID: NCT03176069 Completed - Vaginismus Clinical Trials

Evaluation and Comparison of Women Pelvic Floor With and Without Sexual Dysfunction (Vaginismus)

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Sexuality is considered one of the pillars of quality of life, an integral part of the personality of each individual. Being a basic human being need, it cannot be separated from other aspects of life. For several centuries and until recently, sexuality was considered the "lower instincts" expression related only to the sexual act. Sex is associated with "reproduction" of the sexual energy. On the other hand, the exercise of sexuality includes various factors such as the building of the sensitivity between individuals like touch, dance, fantasy, look, etc. For a long time feminine sexuality was predominantly focused on procreation and has only recently been considered as an integral part of sexual and reproductive rights of women. Vaginismus is a female sexual dysfunction that affects the quality of sexual and psychosocial lives of women, influencing the quality of the couple's relationship. The scientific literature emphasizes the importance of the examination, diagnosis and physical therapy for this dysfunction, but until now there is no quantification or evaluation of the pelvic floor muscles for this group of women, which justifies the realization of this project.

NCT ID: NCT02430038 Completed - Vaginismus Clinical Trials

Transperineal Ultrasound to Assess the Progress of Labour

Start date: April 2015
Phase:
Study type: Observational

This is a prospective observational study of transperineal ultrasound between 24-42 weeks gestation and a prospective longitudinal observational study in all term (37-42 weeks) labouring women.

NCT ID: NCT01859507 Completed - Vaginismus Clinical Trials

Injection of Botox in the Perineal Muscles in Resistant Cases of Vaginal Spasm

VginsmsBOTOX
Start date: January 2013
Phase: N/A
Study type: Interventional

During the first visit, the couple will be acquainted with their condition. This will include the epidemiology of their condition, some sex education tips, as well as the therapeutic modalities available. This is followed by short description of the protocol. In the procedure room, each patient will be examined to determine the degree of vaginismus and classify her condition according to Lemont's classification as modified by Pacik, from 1 to 5. In the same or subsequent sessions, surface anesthesia of the area of injection followed by ice packs is used before the BOTOX is injected into the muscle.

NCT ID: NCT01530113 Not yet recruiting - Depression Clinical Trials

Childhood Sexual Abuse, Vaginismus and Labor Dystocia

CSA-V-LD
Start date: March 2012
Phase: N/A
Study type: Observational

The study aims to develop a theoretical model explicating the inter-relationships between Childhood Sexual Abuse (CSA), Partial Vaginismus (PV) and Labor Dystocia (LD), including their associations with Depression (D) as a mediating variable. The following research hypotheses will be tested: 1. CSA will serve as a risk factor for D, PV and LD. - pregnant women with a history of CSA will have higher levels of D compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have more PV compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have higher levels of LD compared to pregnant women without a history of CSA. 2. D will serve as a mediator between prenatal PV and LD. 3. PV will serve as a risk factor for LD. 4. postpartum PV will be affected by childbirth (LD vs. no LD) contingent on the level of D.