Vulvodynia Clinical Trials

14 recruiting

Frequently Asked Questions

Common questions about Vulvodynia clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 113 of 13 trials

Recruiting
Phase 2

Topical Ketotifen 0.25% for Secondary Vestibulodynia

VulvodyniaProvoked VestibulodyniaSecondary Provoked Vestibulodynia+4 more
Center for Vulvovaginal Disorders54 enrolled3 locationsNCT07257029
Recruiting
Not Applicable

Does a Virtual Program for Pelvic Pain Improve Pain and Sexual Outcomes in Individuals With Provoked Vestibulodynia?

VestibulodyniaVulvodynia (Chronic Vulvar Pain)Vulvar Vestibulitis+2 more
Queen's University250 enrolled1 locationNCT06999395
Recruiting
Phase 2

A Phase 2 Study to Evaluate the Efficacy and Safety of Pudafensine in Vulvodynia (Provoked Vestibulodynia)

Vulvodynia
Initiator Pharma24 enrolled1 locationNCT07391241
Recruiting

Prospective Data Bank Creation to Study Vaginal Conditions

VulvodyniaMycoses
Texas Tech University Health Sciences Center550 enrolled1 locationNCT01829204
Recruiting
Not Applicable

Young Vulvodynia: Effect and Efficacy of Multimodal Treatment.

Vulvodynia
Region Örebro County15 enrolled1 locationNCT07092332
Recruiting
Not Applicable

VIBRating vs Traditional Therapy for Treatment of ENTry Dyspareunia

DyspareuniaVestibulodyniaPelvic Pain+3 more
Medstar Health Research Institute60 enrolled1 locationNCT06840314
Recruiting
Not Applicable

Vulvodynia Intervention: the Effect of Multimodal Treatment for Provoked Vulvodynia

Vulvodynia (Chronic Vulvar Pain)
Karlstad University50 enrolled1 locationNCT06981611
Recruiting
Not Applicable

Biomodulation and Rehabilitation Interventions to TarGet Pelvic Health

VulvodyniaDyspareuniaProvoked Vestibulodynia
University of Ottawa240 enrolled2 locationsNCT06660212
Recruiting

Vestibulodynia At High Resolution: Omics Approach to Improve Diagnosis

VulvodyniaVestibulodynia (VBD)
Fondazione IRCCS Policlinico San Matteo di Pavia400 enrolled1 locationNCT06865963
Recruiting
Not Applicable

Lasertherapy for Vulvodynia

Vulvodynia
Medical University of Graz92 enrolled1 locationNCT04711369
Recruiting
Not Applicable

Acupuncture in a Multidisciplinary Approach for Vulvodynia and Chronic Pelvic Pain

Vulvodynia
Medical University of Graz68 enrolled1 locationNCT05324280
Recruiting
Not Applicable

Vestibulectomy Surgical Techniques Comparison Study

VulvodyniaVulvar Pain
Oregon Health and Science University118 enrolled1 locationNCT05343182
Recruiting
Phase 2

Effectiveness of Low-dose Naltrexone in Patients With Different Types of Vulvodynia

VulvodyniaQuality of LifeNaltrexone
Medical University of Lublin300 enrolled1 locationNCT05955313