Massage therapy shows promise for menstrual cramps
NCT ID NCT07378475
First seen Jun 25, 2026 · Last updated Jul 30, 2026 · Updated 3 times
Summary
This pilot study tests if a gentle massage technique called manual lymphatic drainage (MLD) can reduce period pain in young women aged 18-25 with primary dysmenorrhea. Twenty participants will receive three monthly MLD sessions before their period. Researchers will measure pain, abdominal swelling, and sleep quality.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Manual Lymphatic Drainage (MLD) - a gentle massage technique
- What this could lead to
- If it works, this could offer a drug-free option to reduce period pain and improve quality of life for young women.
- What could go wrong
- This is a very small pilot study (20 people) with no comparison group, so results may not be reliable or apply to everyone. It only tests short-term effects.
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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20 people
The number who actually took part.
- Started
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Jan 2026
- 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 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female participants aged 18-25 years * Confirmed diagnosis of primary dysmenorrhea * Regular menstrual cycles * Ability to provide informed consent Exclusion Criteria: * Secondary dysmenorrhea * Use of hormonal contraceptives * Presence of pelvic pathology (endometriosis, polycystic ovary syndrome, fibroids) * Irritable bowel syndrome * Use of analgesics or anti-inflammatory drugs within 12 hours prior to intervention * Any therapy for dysmenorrhea in the previous month * Pregnancy or suspected pregnancy * Irregular menstrual cycles
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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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University Camilo José Cela
Madrid, 28692, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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