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Study identifier: NCT06840314 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

VIBRating vs Traditional Therapy for Treatment of ENTry Dyspareunia

Condition: Genito-Pelvic Pain/Penetration Disorder · Dyspareunia · Vaginismus  ·  Sponsor: Medstar Health Research Institute

PhaseNA
Planned participants60
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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. Does the use of the Kiwi device lead to higher sexual function scores compared to traditional vaginal dilators 2. Does the Kiwi device improve sexual distress, pain, and overall symptom severity more effectively than traditional vaginal dilators? Researchers will compare the Kiwi vibrating device to traditional cylindrical vaginal dilators to assess whether the Kiwi device results in greater improvements in sexual function and symptom relief. Participants will: * Be randomly assigned to use either the Kiwi device or traditional vaginal dilators. * Use the assigned device three times per week for 15 minutes per session over four weeks. * Complete surveys before and after the study, including assessments of sexual function, pain, and overall improvement.

This description comes directly from the study's public registry record.

Talk to the study team

Helen Y Zhang, MD  ·  202-877-6526  ·  helen.y.zhang@medstar.net

Eun Sook Choi, MD  ·  202-877-6526  ·  eunsook.choi@medstar.net

Always discuss trial participation with your own doctor first.

Locations (1)

MedStar HealthWashington D.C., District of Columbia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06840314