Participants Needed for a Clinical Research study on Vulvodynia

If you are a premenopausal woman over 18 years of age who has had provoked vestibulodynia for at least 6 months, but for no more than 15 years, and never had a vaginal delivery including attempted vaginal delivery, you may be eligible to participate in this study. Patients with deep pain during intercourse are not eligible to participate in this study. Participants also cannot have genitourinary conditions which may interfere with the study, previous surgery that according to investigator’s judgement may impact the study outcome (including but not limited to hysterectomy, vestibulectomy, urologic surgery, perianal surgery) or genital trauma or mutilation/cutting. Participants also must be willing to practice a highly effective form of contraception at the beginning of the study, during the study, and for a minimum of 12 weeks following the last administration of the study drug.

This study will be conducted in the following locations:
  • San Diego, California
  • Washington, DC
  • Kansas City, Missouri
  • Omaha, Nebraska
  • New Brunswick, New Jersey
  • Morristown, New Jersey
  • New Hyde Park, New York
  • Bryn Mawr, Pennsylvania
  • Nashville, Tennessee
  • Seattle, Washington
  • Cincinnati, Ohio
  • Pompano Beach, Florida
  • Miami, Florida
If you are interested in participating, please email  clinical.trials@ipsen.com. For more information on the study, please go to  https://clinicaltrials.gov/ct2/show/NCT03598777. For information on more vulvodynia studies looking for participants, please go to https://www.nva.org/for-patients/participate-in-research/.