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The effect of probiotics supplementation in women with dysmenorrhea: a randomized controlled study

Phase 2
Recruiting
Conditions
women with dysmenorrhea aged 18-24 years
dysmenorrhea
probiotics
Registration Number
TCTR20230326001
Lead Sponsor
Ramathibodi hospital, Mahidol University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
48
Inclusion Criteria

1 moderate dysmenorrhea
2 regular menstruation cycle
3 aged 18-24 years old
4 All patients need to write and sign a written informed consent.

Exclusion Criteria

Exclusion Criteria
1. Detecting a pathology in the pelvic organs from pelvic examination or ultrasound
2. History of other medical condition both acute and chronic diseases or have a congenital disease that requires regular medication including psychiatric diseases
3. Menstrual pain score less than 5 as assessed by VAS.
4. History of abdominal surgery
5. History of being diagnosed with a pelvic infection or sexually transmitted disease
5. History of using hormonal contraceptives or IUDs in the 6 months prior to study participation.
6 History of pregnant, miscarried, delivered a child, or were in the planning stages of pregnancy?
7. Take other dietary supplements, herbs, and vitamins 6 months before participating in the study.
8. Refusing to participate in a research project or withdrawing from the study.
9 .Have a history of allergy to powder or components of probiotics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
dysmenorrhea 3 months Visual analogue scale
Secondary Outcome Measures
NameTimeMethod
premenstrual symptoms 3 months PSST,Frequency of Non-steroidal Anti-Inflammatory Drugs (NSAIDs) use between placebo and probiotic group 3 months number of tablets,quality of life 3 months questionnaire
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