Can needles ease PMS? a trial puts electroacupuncture to the test
NCT ID NCT07737210
First seen Jul 30, 2026 · Last updated Jul 31, 2026 · Updated 1 time
Summary
This trial investigates whether adding electroacupuncture to a daily nutritional supplement can reduce the severity of premenstrual syndrome (PMS) in young women aged 20 to 29. Participants receive either the supplement alone or the supplement plus 21 sessions of electroacupuncture over three menstrual cycles. The study measures changes in PMS symptoms and blood progesterone levels to see if the combination offers greater relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- electroacupuncture combined with a nutritional supplement (calcium, magnesium, vitamin B6, zinc)
- What this could lead to
- If effective, electroacupuncture could offer a drug-free option to reduce PMS symptoms in young women.
- What could go wrong
- This is a small, early-stage trial with 60 participants, so results may not apply broadly. Electroacupuncture is generally safe but may cause mild 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
-
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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60 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Jan 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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20 to 29 years
- Sex
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Female participants only
- Healthy volunteers
-
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 diagnosed with or suffering from premenstrual syndrome. * Regular menstrual cycles. * Age from 20 to 29 years. * Body mass index (BMI) from 25 to 29.9 kg/m². * Single, virginal, and non-smoking participants. Exclusion Criteria: * Cardiorespiratory, renal, neurological, pelvic inflammatory, thyroid, or mental disorders. * Anemia, diabetes mellitus, hypertension, asthma, rheumatoid arthritis, headache, or migraine. * Acupuncture treatment during the preceding six months. * Pregnancy or intention to become pregnant. * Participation in another exercise or training program during the study. * Use of medications or hormonal treatment that could influence the study outcomes.
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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
-
Cairo university
Cairo, Egypt
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Other studies related to the condition(s) this trial covers.
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