Long-Term Assessment of Quality of Life and Effectiveness of Onabotulinumtoxina Injections in Provoked Vestibulodynia

Centre Hospitalier Universitaire de Besancon21 enrolled

Overview

The study aims to assess and compare the pain in women suffering from provoked vestibulodynia, before treatment with botulinum injections, 3 months after treatment and 18 months after treatment.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Vestibulodynia

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Vestibulodynia rated B2 according to 2003 International Society for the Study of Vulvovaginal Disease (ISSVD) classification * Patients previously treated no later than18 months ago for provoked vestibulodynia with botulinum toxin injections, in the University Hospital of Besançon. Exclusion Criteria: * Major psychologic disorders.

Locations (1)

CHU Besançon

Besançon, France

Outcomes

Primary Outcomes

Long-term pain improvement after botulinum toxin injections

Assessment and comparison of pain using Visual Analogic Scale values before treatment,3 months after treatment and 18 months after treatment.

Time frame: 18 months

Data from ClinicalTrials.gov

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