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Effectiveness of a Four-Session Focal Shock Wave Therapy Protocol in Women With Vulvodynia

Recruitingn/aAges 18 Years - anyFemaleNantes University Hospital
NCT07553715 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
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
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What it tests

  • Low-Intensity Focal Extracorporeal Shock Wave Therapy
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Where

1 site
CHU Nantes- Allergy Department
Nantes, France
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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