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NCT07553715
Effectiveness of a Four-Session Focal Shock Wave Therapy Protocol in Women With Vulvodynia
Conditions: Vulvodynia
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 50
Sponsor: Nantes University Hospital
Location: CHU Nantes- Allergy Department Nantes Nantes
Summary
Vulvodynia is a chronic vulvar pain condition that can significantly affect quality of life. Low-intensity focal extracorporeal shock wave therapy has been proposed as a non-invasive therapeutic option, but real-world data remain limited.
This retrospective observational study aims to evaluate the effectiveness of a four-session focal shock wave therapy protocol in women with vulvodynia treated in routine clinical practice at a university hospital. Clinical data collected during standard care, as well as questionnaire responses, will be analyzed to assess changes in symptoms and functional outcomes following treatment.
Eligibility Criteria
Inclusion Criteria:
* Female patients aged 18 years or older
* Clinical diagnosis of vulvodynia
* Received at least one session of low-intensity focal extracorporeal shock wave therapy in routine clinical practice
Exclusion Criteria:
* Refusal to participate (non-opposition not obtained)
* Inability to understand French language, preventing completion of study questionnaires
Source: ClinicalTrials.gov (NCT07553715). StuddyBuddy aggregates publicly available trial information.