CompletedPhase 2ketamine

Novel Topical Therapies for the Treatment of Genital Pain

NCT ID

NCT02099006

Target Enrollment

9 participants

Start Date

2013-11

Est. Completion

2015-06

About This Study

This study is testing drugs not previously used topically for the treatment of vulvodynia, a common genital pain syndrome. It is hoped that one of these drugs will improve vaginal entryway pain with touch, daily pain scores and sexual functioning.

Conditions Studied

Female Genital Diseases

Interventions

•Amitriptyline
•Baclofen
•Ketoprofen
•Ketamine
•Loperamide
•Gabapentin
•placebo

Eligibility

Sex:FEMALE

Age:18 Years - 65 Years

Healthy Volunteers:No

View full eligibility criteria

Inclusion Criteria:

* Women between ages of 18 and 65 who complain of localized provoked vulvar pain and meet the criteria for the diagnosis of localized provoked vulvodynia. Patients who have failed or have been unable to tolerate previous attempts at systematic therapy or surgery will be specifically recruited.

Exclusion Criteria:

1. The presence of a dermatologic or neurologic condition which is determined by the investigator to be the primary cause of the patient's pain.
2. Allergy to any of the medications or the base itself.
3. Concurrent use of the following medications. . The patient may enroll in the study after a two week washout from these medications. Patients may need to receive approval from the prescribing physician before stopping these medications. Failure to obtain approval for medication cessation would be cause for exclusion.

Gabapentin (NeurontinTM) Amitriptyline (ElavilTM) Nortriptyline (PamelorTM) Desipramine (NorpraminTM) Tramadol (UltramTM, ConZipTM, RybixTM, RysoltTM, Ultram ERTM) Pregabalin (LyricaTM) Baclofen

Study Locations (1)

University of Rochester

Rochester, New York, United States