A cup of lavender tea a day may keep PMS blues away — science puts it to the test
NCT ID NCT07737366
First seen Jul 30, 2026 · Last updated Sep 18, 2026 · Updated 2 times
Summary
This trial tests whether drinking lavender herbal tea twice daily for nine days around each menstrual cycle can reduce the emotional and physical symptoms of premenstrual syndrome (PMS), such as anxiety, depression, stress, and pain. Sixty women with PMS will be randomly assigned to drink lavender tea or to a waiting-list control group. Researchers will measure changes in PMS symptoms, quality of life, and menstrual bleeding over two cycles.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lavender herbal tea
- What this could lead to
- If effective, lavender tea could offer a natural, low-cost option for women to manage PMS symptoms at home.
- What could go wrong
- This is a small, early-stage trial with 60 participants. The effects may be modest, and lavender tea is not a substitute for medical treatment.
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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Jul 2025
- Finished
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Oct 2025
- 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 years and older
- 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: * No history of acute or chronic illness, Meeting the diagnostic criteria for PMS specified by ACOG, Over 18 years of age, No psychiatric distress and no treatment for psychiatric distress in the last 3 months, No (current or past) participation in psychotherapy for premenstrual symptoms, Not pregnant, Gynecological diseases (hysterectomy, oophorectomy, gynecological cancer, polycystic ovary syndrome, endometriosis, infertility) are among the inclusion criteria. Exclusion Criteria: * Allergy to any herbal tea, food or medicine, Psychiatric illness or chronic illness, Use of psychiatric medication (such as anxiolytics and antidepressants), Regular medication use (such as antihypertensive, antidiabetic), Regular use of herbal teas or complementary medicines, Failure to meet the diagnostic criteria for PMS specified by ACOG, No regular menstruation in the last 3 months, Use of oral contraceptives during the last 3 months, Use of analgesics during menstruation while participating in the study.
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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
-
Sakarya University
Sakarya, 54050, Turkey (Türkiye)
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