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The impact of ginger and curcumin on severty of premenstural syndrome symptoms

Not Applicable
Conditions
premenstrual syndrome.
Premenstrual tension syndrome
Registration Number
IRCT201301012751N7
Lead Sponsor
ursing and Midwifery Faculty of Tehran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
105
Inclusion Criteria

Regular menstrual cycles 21-35 days, 18-35 years of age , unmarried, Physical and mental health , non-hormonal drugs, anticoagulant, antidepressants, supplements and herbal medicine, Not sensitive to turmeric and ginger , not taking any medication for the treatment of premenstrual syndrome, No alcohol or drugs, Non-traumatic stress in the last 3 months, no surgery in the last 3 months.
Exclusion criteria: Unwillingness to continue participation in the study , If complications or allergic to a drug or other drug use, If stop taking the medication or taking medication irregularly , Identification of any disease such as endocrine disease, married during the study , Menstrual cycle irregularity during the study , Stressful events occurred during the study

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in physical symptoms (headache, breast swelling and tenderness, back pain, abdominal pain, muscle pain, weight gain, swelling of extremities, nausea, diarrhea or constipation). Timepoint: One month, two months, three months after intervention. Method of measurement: Questionnaire.;Reduction in mood symptoms (irritability and restlessness, anxiety and impatience, anger, depression and sadness, crying for no reason, feeling alone). Timepoint: One month, two months, three months after intervention. Method of measurement: Questionnaire.;Reduction in behavioral symptoms (fatigue, lack of energy, insomnia, difficulty concentrating, increased appetite). Timepoint: One month, two months, three months after intervention. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Side effects of drugs. Timepoint: Three months after the intervention. Method of measurement: Questionnaire.
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