Efficacy of a Physiotherapy Treatment in Women Suffering From Provoked Vestibulodynia

• Status: Completed
• Trial end date: 2015-11-01
• Target enrollment: 0
• Participant gender: Female

Summary

Chronic gynaecological pain is a major medical problem that affects 20-30% of women at different moments of their life. This largely neglected issue has a significant impact on the sexual and conjugal life of women suffering from it as well as on their psychological health. Furthermore, this kind of pain is not well understood, often misdiagnosed or even totally ignored. Also, treatment is limited and not extensively studied. This study aims at better understanding and treating gynaecological pain. The focus of the study will be provoked vestibulodynia, pain at the entry of the vagina. The efficacy of specialized pelvic floor physiotherapy will be compared to a topical cream (lidocaine) applied to the vulva. The treatment efficacy will be assessed in 234 women (aged from 18-45 years old) suffering from provoked vestibulodynia recruited in 4 hospitals (CHUS, Jewish General Hospital, Royal-Victoria Hospital, CHUM St-Luc).

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Université de Sherbrooke
• Collaborators: Canadian Institutes of Health Research (CIHR); Fonds de la Recherche en Santé du Québec
• Treatments: Lidocaine

Criteria

Inclusion Criteria:

• Moderate to severe pain in at least 90% of sexual intercourses.

• Moderate to severe pain during the cotton-swab test at one of more vestibule regions (5/10 minimum pain evaluation on the verbal pain intensity scale).

• Pain limited to the vestibule during vaginal penetrations and during activities applying pressure on the vestibule.

• Provoked vestibulodynia lasting at least 6 months prior to the study and diagnosed by a standardised gynaecologic exam protocol by one of our collaborator.

Exclusion Criteria:

• Major psychiatric condition or pelvic pathology associated with a genital pain problem (e.g.: dyspareunia).

• Use of medication that could influence pain perception.

• Actual or past pregnancy.

• Vulvar or vaginal surgery

• Post-menopausal state

• Unwillingness to restrain from other treatments till the 6 months post-treatment evaluation.

• Urogynaecologic symptoms (urinary/anal incontinence, pelvic organs prolapsus, urinary/vaginal infection active or during the last 3 months).

• Incapacity to have sexual intercourse including vaginal penetration during the last 6 months.

• Physiotherapy treatments or lidocaine application prior to the study