Clinical Trial

Young Vulvodynia: Effect and Efficacy of Multimodal Treatment.

Study acronym: UV
Active, Not Recruiting
View on ClinicalTrials.gov →
Summary
The aim of this SCED-study is to evaluate a multimodal treatment for vulvodynia in young women. The main questions it aims to answer are: Is multimodal treatment effective for provoked vulvodynia in young women? How is multimodal treatment experienced by young women with vulvodynia? Participants will respond to frequent questionnaires (two times a week) during a baseline period of 4,5 or 6 weeks, as well as during their treatment period ( a total of 25 weeks). In addition they will respond to pre-, post-treatment and 6 month follow-up questionnaires.
Protocol Amendment History 1 change
critical Enrollment closed, study ongoing 2026-08-13
Trial Details
NCT Number NCT07092332
Lead Sponsor Region Örebro County
Collaborators: Örebro University, Sweden
Conditions Vulvodynia
Enrollment 15 participants
Start Date 2025-06-10
Primary Completion 2026-12-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-12