Recruiting NA Genito-Pelvic Pain/Penetration Disorder

Compares treatment options for Genito-Pelvic Pain/Penetration Disorder

Official title VIBRating vs Traditional Therapy for Treatment of ENTry Dyspareunia

ClinicalTrials.gov ID: NCT06840314

What this study is testing

What it's testing
The goal of this randomized controlled trial is to determine whether the use of a novel vibrating pelvic floor therapeutic device ("Kiwi") improves sexual function in sexually active women aged 18 and older with genito-pelvic pain and penetration disorder (GPPPD) more effectively than traditional vaginal dilators. The main questions it aims to answer are: 1.
  • Which group you join is decided by chance.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older, women only

You may be able to join if

  • Assigned female at birth
  • Age ≥ 18 years old
  • Genito-pelvic pain/penetration disorder (per ICD-10 diagnosis codes: F52.5 Vaginismus not due to a substance or known physiological condition, F52.6...

You likely can't join if

  • Current or prior use of a therapeutic vaginal device used to treat GPPPD
  • Unmanaged genitourinary syndrome of menopause
  • History of pelvic radiation
  • History of genital tract malignancy
  • History of female genital mutilation
  • History of prior surgery for prolapse or incontinence, including vaginal mesh or midurethral sling mesh
See the full eligibility criteria
Who can join
  • Assigned female at birth
  • Age ≥ 18 years old
  • Genito-pelvic pain/penetration disorder (per ICD-10 diagnosis codes: F52.5 Vaginismus not due to a substance or known physiological condition, F52.6 Dyspareunia not due to a substance or known physiological condition...
What rules you out
  • Current or prior use of a therapeutic vaginal device used to treat GPPPD
  • Unmanaged genitourinary syndrome of menopause
  • History of pelvic radiation
  • History of genital tract malignancy
  • History of female genital mutilation
  • History of prior surgery for prolapse or incontinence, including vaginal mesh or midurethral sling mesh
  • Silicone allergy

The study team makes the final eligibility decision.

Where it's taking place

  • Washington D.C., District of Columbia, United States

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Washington D.C., District of Columbia, United States. Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.