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RECRUITING
NCT07553715

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

Sponsor: Nantes University Hospital

View on ClinicalTrials.gov

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.

Official title: Evaluation of the Effectiveness of a Four-Session Low-Intensity Focal Extracorporeal Shock Wave Therapy (LiSWT) Protocol in Women With Vulvodynia: A Retrospective Observational Cohort Study

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2026-04-01

Completion Date

2026-12-01

Last Updated

2026-06-24

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Low-Intensity Focal Extracorporeal Shock Wave Therapy

Low-intensity focal extracorporeal shock wave therapy delivered using a medical device (Duolith SD1, Storz Medical). The protocol consisted of four treatment sessions performed in routine clinical practice, typically at weekly intervals. Treatment parameters followed standard clinical settings used for vulvodynia management.

Locations (1)

CHU Nantes- Allergy Department

Nantes, Nantes, France