54 Participants NeededMy employer runs this trial

IncobotulinumtoxinA for Vulvodynia

Recruiting at 1 trial location
AG
Overseen ByAndrew Goldstein, MD
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a treatment called incobotulinumtoxinA (a type of botulinum toxin injection) to determine its effectiveness for provoked vestibulodynia, a condition causing pelvic pain due to tight muscles. Researchers aim to assess whether this treatment can safely reduce pain during certain activities. The trial compares the treatment to a placebo (a non-active substance) to evaluate its effectiveness. Ideal candidates for this trial are premenopausal women who have experienced pain triggered by touch in the pelvic area for at least three months and report significant discomfort during testing. As a Phase 2 trial, this research focuses on measuring the treatment's effectiveness in an initial, smaller group, allowing participants to contribute to important early findings.

Do I have to stop taking my current medications for the trial?

The trial requires that if you are taking oral antidepressants, anxiolytics, or anti-epileptics, your dose must have been stable for at least 3 months before starting the trial and should remain stable throughout the study. If you are undergoing pelvic floor physical therapy, the frequency of visits should also be stable for at least 8 weeks before the trial and remain stable during the study.

Is there any evidence suggesting that incobotulinumtoxinA is likely to be safe for humans?

Research has shown that incobotulinumtoxinA is generally safe and effective for treating pelvic and vulvar pain. In studies involving over 2,600 patients, the treatment maintained its effectiveness over time without resistance. One study found that even at high doses, it did not cause serious side effects. Some patients might experience mild reactions, such as temporary muscle weakness or soreness, but these are uncommon. Overall, the evidence suggests that incobotulinumtoxinA is safe for managing pain related to pelvic floor disorders.12345

Why do researchers think this study treatment might be promising for vulvodynia?

Researchers are excited about IncobotulinumtoxinA for vulvodynia because it offers a novel approach compared to standard treatments like oral medications and topical creams. Unlike these traditional methods, IncobotulinumtoxinA works by targeting the nerve pathways responsible for pain, potentially providing relief through a different mechanism of action. This unique approach could lead to more effective pain management and improved quality of life for those suffering from vulvodynia. Additionally, as a targeted injection, it may offer quicker relief compared to treatments that require prolonged use.

What evidence suggests that incobotulinumtoxinA might be an effective treatment for vulvodynia?

Research has shown that incobotulinumtoxinA, a type of botulinum toxin, may help treat provoked vestibulodynia (PVD), a painful condition affecting the vulva. Studies have found that botulinum toxin can ease pain by relaxing the tight pelvic floor muscles that cause PVD. In one study, patients experienced significantly less pain after receiving botulinum toxin injections. Another review noted its success in improving related issues like painful intercourse and ongoing pelvic pain. Overall, this evidence suggests that incobotulinumtoxinA, which participants in this trial may receive, could effectively reduce pain for people with PVD.12678

Are You a Good Fit for This Trial?

This trial is for premenopausal women aged 18 or older with a confirmed diagnosis of provoked vestibulodynia (pain in the vaginal opening triggered by touch) and overactive pelvic floor muscles. They must have significant pain during testing, be able to use small dilators, and not have had recent botulinum toxin injections or certain other pelvic conditions.

Inclusion Criteria

I am a woman who is 18 years old or older.
* Willing to provide a written informed consent prior to any study related procedures.
* Have provoked pain at the posterior vestibule on a cotton swab test, with pain at positions 4, 6 and 8 o'clock (must be bilateral pain) at the Baseline Visit.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive incobotulinumtoxinA or placebo for the treatment of provoked vestibulodynia

24-30 weeks
Regular visits for treatment and assessment

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • IncobotulinumtoxinA

Trial Overview

The study compares incobotulinumtoxinA (a type of botox injection) to a placebo shot for treating pain caused by provoked vestibulodynia linked to tight pelvic floor muscles. Participants are randomly assigned to either group without knowing which treatment they receive.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: INA groupExperimental Treatment1 Intervention
Group II: Placebo GroupPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Center for Vulvovaginal Disorders

Lead Sponsor

Trials
8
Recruited
270+

Merz Pharmaceuticals

Industry Sponsor

Trials
6
Recruited
460+

Citations

Clinical impacts of botulinum toxin type A injections for ... - PMC

This meta-analysis evaluated the efficacy and safety of botulinum neurotoxin type A injections for the treatment of provoked vestibulodynia.

(117) Incobotulinumtoxina for Provoked Vestibulodynia With ...

This study addresses a major therapeutic gap in vulvodynia care by evaluating a targeted treatment for women whose provoked pain is driven by ...

Treatment of Vestibulodynia with Submucosal Injections of ...

The results indicate the beneficial effects of BoNT/A in treating vestibulodynia and reinforce the importance of adapting the treatment according to its ...

(117) Incobotulinumtoxina for Provoked Vestibulodynia ...

Conclusions This study addresses a major therapeutic gap in vulvodynia care by evaluating a targeted treatment for women whose provoked pain is ...

Botulinum toxin for provoked vestibulodynia - Kim, S - 2025

There is evidence from observational studies suggesting that botulinum toxin is a potentially effective treatment for PVD. There are several ...

Clinical Evidence & Trial Data

In pivotal trials with over 2,600 patients, XEOMIN delivered results with 0% treatment resistance due to neutralizing antibodies.1. Actual patient. Individual ...

Botulinum toxin injection in vulva and vagina. Evidence ...

On this regard, we aimed assessing the therapeutic effectiveness and safety of BoNT usage in the treatment of vaginal, vulvar and pelvic pain disorders. Methods.

Investigation of Efficacy of incobotulinumtoxinA (Xeomin) in ...

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure.