Ultrasound-Guided needle therapy may ease menstrual cramps
NCT ID NCT07176910
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether a technique called Doppler-guided angiopuncture can safely reduce pain in women with primary dysmenorrhea (period pain). Researchers will perform the needle procedure on 30 participants and measure pain changes using a standard pain scale. The goal is to see if this approach offers a new way to manage menstrual cramps without medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- angiopuncture (a needle procedure guided by Doppler ultrasound)
- What this could lead to
- If it works, this could offer a new, non-drug option for managing period pain.
- What could go wrong
- This is a very small early trial with only 30 people, so results may not apply widely. The procedure involves needles and carries minor risks like bruising or infection.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2024
- Expected to finish
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Nov 2025
An estimate. End dates often move.
- 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 25 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: Primary dysmenorrhea diagnosis (≥6 months of menstrual pain scoring ≥2 on numerical rating scale) Regular menstrual cycles (28-32 days), menstrual period lasts 4 to 7 days No pelvic pathology on transvaginal ultrasound. Exclusion Criteria: coagulopathy (INR \>1.5) recent analgesic use (48-hour washout) secondary dysmenorrhea confirmed by laparoscopy.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The Third Affiliated Hospital of Changchun University of Chinese Medicine
RECRUITINGChangchun, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can pelvic floor exercises plus taping or electrical current ease period pain?
- Can a tiny patch tame period pain without drugs?
- Can learning about pain make exercise work better for period cramps?
- Ancient heat therapy put to the test for menstrual cramps
- Could childhood trauma shape period pain in adulthood?
- Could a school program ease teen period pain without pills?