Good bacteria vs. bad cramps: probiotics tested for menstrual relief
NCT ID NCT07530081
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether taking a daily probiotic supplement can reduce menstrual pain and premenstrual symptoms in women. 150 women with moderate-to-severe period pain will take either a high or low dose of probiotics or a placebo for four menstrual cycles. Researchers will track changes in pain, mood, and sleep quality using standard questionnaires.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Probiotic (Lactobacillus rhamnosus F-1)
- What this could lead to
- If it works, this could offer a natural, side-effect-free option for managing period pain and premenstrual symptoms.
- What could go wrong
- This is a small, early-stage trial with no phase designation. Probiotics may not outperform placebo, and results may not apply to everyone.
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
-
150 people
The number who actually took part.
- Started
-
Mar 2024
- Expected to finish
-
Jun 2026
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 65 years
- Sex
-
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: * Female aged between 20 and 65 years. * Regular menstrual cycles. * During the last three menstrual periods, self-reported dysmenorrhea with a pain score ≥ 3 on the Numeric Rating Scale (NRS). * Able to use effective contraception during the study period. * Willing to participate in the study and has signed the informed consent form. Exclusion Criteria: * Planning to become pregnant, currently pregnant, or in the postpartum stage with menstruation not yet resumed. * Postmenopausal women. * Irregular menstrual cycles (cycle length \< 21 days or \> 40 days). * Currently taking any psychiatric medications, oral contraceptives, menstrual regulation drugs, weight-loss drugs, or antibiotics. * Consumption of probiotic-related products within the past 1 month (including drops, tablets, capsules, powder, or yogurt and fermented milk products).
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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
-
China Medical University Hospital
Taichung, 404, Taiwan
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Other studies related to the condition(s) this trial covers.
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