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Not feasible due to low accrual
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The purpose of this study is to determine whether pregabalin is effective in the treatment of vulvodynia.
Vulvodynia is a condition exclusive to women and involves mostly burning, rawness, and itching of the external genitourinary tract that often results in painful intercourse. Vulvodynia rarely results in severe morbidity or mortality; rather it causes symptoms of the lower genital, urinary, and gastrointestinal tracts that can impact a woman's daily activities and negatively affect her quality of life.
Despite the fact that chronic vulvovaginal symptoms are one of the most common reasons for visits to a gynecology clinic, epidemiologic studies of the incidence and prevalence of these conditions are rare and available population-based studies are limited. Approximately 16% of women will experience chronic vulvar pain at some point in their lifetime; with 5% experiencing this condition before age 25.
Treatment approaches include behavioral changes, medical management, and surgery, specifically vulvar vestibulectomy. Prior to considering surgical intervention, all medical treatment options should be exhausted. Although vulvodynia is quite prevalent and can be a debilitating disease, there are few studies that critically evaluate the medical management of vulvodynia. Pregabalin is an anticonvulsant that has proven efficacy in the treatment of diabetic neuropathy, post-herpetic neuralgia, and fibromyalgia. Anecdotal data and one case report provide hope that this medication may also be effective in the treatment of vulvodynia.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| pregabalin/placebo | Experimental | pregabalin and placebo given using a cross-over design |
|
| placebo/pregabalin | Experimental | placebo and pregabalin given using a cross-over design |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| pregabalin | Drug | pregabalin 150mg twice daily for 4 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in Average Pain Over the Last 7 Days of Each Arm Using an 11-point Scale (0-10) | The primary objective of this protocol is to compare the reduction in pain using an 11-point scale (0-10) at four weeks of treatment. A responder will be defined as a subject noting a ≥50% reduction in pain using this scale. The NRS is an 11-point scale comprising a number from 0 through 10; 0 indicates "no pain", and 10 indicates the "worst imaginable pain". Outcomes measure not assessed due to early discontinuation because of poor recruitment. As such, the study was terminated prior to the designated follow up interval. Therefore, no outcomes data was collected. | 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Effect on Anxiety and Depression in Women With Vulvodynia Based on the Kessler Psychological Distress Scale (K10) | Subjects will complete the Kessler Psychological Distress Scale (K10). It is a measure of psychological distress. Scores will range from 10 to 50, with the higher the score, the higher the mental distress Data not measured due to early discontinuation of the study prior to the designated follow up time frame. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Beri M Ridgeway, MD | The Cleveland Clinic | Principal Investigator |
| Matthew D Barber, MD, MHS | The Cleveland Clinic | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cleveland Clinic | Cleveland | Ohio | 44195 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | Pregabalin First 4 Weeks | pregabalin and placebo given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
| FG001 | Placebo First 4 Weeks | placebo and pregabalin given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Phase 1: Initial Intervention |
|
| ||||||||||||||||||
| Phase 2: Cross Over |
|
No study analysis completed due to early termination due to poor enrollment
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| ID | Title | Description |
|---|---|---|
| BG000 | Pregabalin First 4 Weeks | pregabalin and placebo given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
| BG001 | Placebo First 4 Weeks | placebo and pregabalin given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Reduction in Average Pain Over the Last 7 Days of Each Arm Using an 11-point Scale (0-10) | The primary objective of this protocol is to compare the reduction in pain using an 11-point scale (0-10) at four weeks of treatment. A responder will be defined as a subject noting a ≥50% reduction in pain using this scale. The NRS is an 11-point scale comprising a number from 0 through 10; 0 indicates "no pain", and 10 indicates the "worst imaginable pain". Outcomes measure not assessed due to early discontinuation because of poor recruitment. As such, the study was terminated prior to the designated follow up interval. Therefore, no outcomes data was collected. | Outcomes measure not assessed due to early discontinuation because of poor recruitment. As such, the study was terminated prior to the designated follow up interval. Therefore, no outcomes data was collected. | Posted | 4 weeks |
|
4 weeks
Data not collected. Long term follow up not available for adverse events as study was discontinued early.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Pregabalin/Placebo | pregabalin and placebo given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Lynn Borzi (Research Administrator) | Cleveland Clinic | 216-445-3158 | BORZIL@ccf.org |
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| ID | Term |
|---|---|
| D056650 | Vulvodynia |
| D054515 | Vulvar Vestibulitis |
| ID | Term |
|---|---|
| D014845 | Vulvar Diseases |
| D005831 | Genital Diseases, Female |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| ID | Term |
|---|---|
| D000069583 | Pregabalin |
| ID | Term |
|---|---|
| D005680 | gamma-Aminobutyric Acid |
| D000613 | Aminobutyrates |
| D002087 | Butyrates |
| D000144 | Acids, Acyclic |
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| 4 weeks |
| NOT COMPLETED |
|
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
pregabalin and placebo given using a cross-over design
pregabalin: pregabalin 150mg twice daily for 4 weeks
| OG001 | Placebo/Pregabalin | placebo and pregabalin given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks |
|
| Secondary | Effect on Anxiety and Depression in Women With Vulvodynia Based on the Kessler Psychological Distress Scale (K10) | Subjects will complete the Kessler Psychological Distress Scale (K10). It is a measure of psychological distress. Scores will range from 10 to 50, with the higher the score, the higher the mental distress Data not measured due to early discontinuation of the study prior to the designated follow up time frame. | Data not measured due to early discontinuation of the study prior to the designated follow up time frame. | Posted | 4 weeks |
|
|
| 0 |
| 8 |
| 0 |
| 8 |
| EG001 | Placebo/Pregabalin | placebo and pregabalin given using a cross-over design pregabalin: pregabalin 150mg twice daily for 4 weeks | 0 | 8 | 0 | 8 |
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| D000091642 | Urogenital Diseases |
| D000091662 | Genital Diseases |
| D014847 | Vulvitis |
| D002264 |
| Carboxylic Acids |
| D009930 | Organic Chemicals |
| D000596 | Amino Acids |
| D000602 | Amino Acids, Peptides, and Proteins |