Can needles quiet chronic pelvic pain?
NCT ID NCT05324280
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study asks whether adding acupuncture to a multidisciplinary treatment plan can reduce pain and improve quality of life for women with vulvodynia or chronic pelvic pain lasting at least six months. Half of the participants will receive acupuncture sessions, while the other half will be placed on a waiting list. Researchers will compare changes in pain scores and quality-of-life questionnaires between the two groups.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Acupuncture (body and ear acupuncture) as part of a multidisciplinary treatment
- What this could lead to
- If effective, acupuncture could become a standard part of multidisciplinary care to help women manage chronic pelvic pain and vulvodynia.
- What could go wrong
- This is a small, early-stage trial, and the waiting-list design may overestimate benefits. Acupuncture is generally safe but may cause minor bruising or discomfort.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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45 people
The number who actually took part.
- Started
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Jun 2022
- Finished
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Jul 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 80 years
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Department of Gynecology/ Medical University of Graz
Graz, 8036, Austria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- WorkoutCPP: a pilot series of N-of-1 trials evaluating RL-Generated adaptive exercise recommendations for pelvic pain management
- Light therapy for pelvic pain: a 1,000-Patient registry seeks answers
- Could gene switches explain chronic pelvic pain?
- Light therapy inside the body: a new hope for chronic pelvic pain?
- Can a laser beam silence chronic vulvar pain?
- A new approach to vulvar pain: could education and behavior change bring relief?