Effects of Chamomile With L-theanine Beverage Among Young Women Experiencing Primary Dysmenorrhea
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Chamomile (Matricaria recutita), Chamomile.
- Who it may be relevant to
- Registry conditions: Primary Dysmenorrhea. Basic parameters: 18 years — 30 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Malaysia
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
This study aims to evaluate the effects of a beverage containing chamomile and L-theanine on menstrual symptoms, pain intensity, mood, and sleep quality among young adult females with primary dysmenorrhea.
Detailed description
This study aims to evaluate the effects of a beverage containing chamomile and L-theanine on menstrual symptoms, pain intensity, mood, and sleep quality among young adult females with primary dysmenorrhea.
Interventions
- Dietary supplement Chamomile (Matricaria recutita)
Participants in the intervention group will consume the chamomile with L-theanine (CTT) beverage, which contains 480 mg of chamomile extract and 200 mg of L-theanine. - Dietary supplement Chamomile
A chamomile-flavored beverage
Primary outcome measures
- Pain intensity [Time frame: 2 months]
- Menstrual symptoms [Time frame: 2 months]
- Sleep quality [Time frame: 2 months]
- Mood [Time frame: 2 months]
Secondary outcome measures (1)
- Hemoglobin [Time frame: 2 months]
Eligibility criteria
Inclusion criteria
- A VAS score of ≥4 cm for the past three consecutive menstrual cycles
- Regular monthly menstruation
- No history of allergies or psychological/gynecological illnesses
- Absence of secondary dysmenorrhea
- No current use of any medications
- No ongoing non-pharmacological management for dysmenorrhea.
Exclusion criteria
- Pregnant
- Breastfeeding
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Supportive care
Study locations
Malaysia · 1 center
- UTAR — Kampar
Identifiers
NCT: NCT07092878 · 78-373