Acupuncture for treating vulvodynia and chronic pelvic pain
Acupuncture in a Multidisciplinary Approach for Vulvodynia and Chronic Pelvic Pain
This study is testing whether acupuncture can help women with vulvodynia and chronic pelvic pain feel better as part of their treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 68 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | Female |
| Sponsor | Medical University of Graz Academic / other |
| Locations | 1 site (Graz) |
| Trial ID | NCT05324280 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of acupuncture as part of a multidisciplinary treatment approach for women suffering from vulvodynia and chronic pelvic pain. Participants will be randomly assigned to either an acupuncture group or a waiting list control group. The study will assess outcomes such as subjective pain perception and health-related quality of life through questionnaires. A total of 68 patients will be recruited from a university outpatient clinic for this randomized controlled clinical study.
Who should consider this trial
Good fit: Ideal candidates for this study are women with vulvodynia and/or chronic pelvic pain lasting at least six months who have undergone multidisciplinary treatment for at least three months.
Not a fit: Patients who are pregnant, have current malignancies, major neurologic or psychiatric conditions, or are participating in another related trial may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a new, effective treatment option for women suffering from vulvodynia and chronic pelvic pain.
How similar studies have performed: Other studies have shown promising results with acupuncture for chronic pain conditions, suggesting potential success for this approach, although this specific application may be novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women with vulvodynia and/or chronic pelvic pain of at least 6 months duration * multidisciplinary treatment for at least 3 months Exclusion Criteria: * Pregnancy * Current malignancy * Major neurologic or psychiatric morbidity * Study participation in Lydia trial (Lasertherapy for vulvodynia)
Where this trial is running
Graz
- Department of Gynecology/ Medical University of Graz — Graz, Austria (Recruiting)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.