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The Impact Of Valerian Root Extract On Pre Menstural Syndrome Symptoms

Not Applicable
Conditions
Premenstural Syndrome.
Unspecified behavioural syndromes associated with physiological disturbances and physical factors
Registration Number
IRCT201211179463N5
Lead Sponsor
Tehran University of Medical Science, vice chancellor for research(primary sponsor
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
100
Inclusion Criteria

Single, 18-35 years, Having regular menstrual cycles and normal 21-35 and Duration of 7-3 days in the last 6 months, Lack of physical and emotional illness known And use of a Use of certain medications, no Occurrence of stressful events during the 3 months before study And diagnosis of premenstrual syndrome according to the Daily Form, Failure to participate in research studies of similar. Exclusion criteria of the study, Lack of volunteers willing to Continued drug use, Occurrence drug allergies, Stopping the medication for a week in the first cycle and irregular use of medication in cycles 2 and 3 for two days, Understanding of physical and mental illness during the study, Married during the study, Relatives death relatives and had surgery during the past two months. and third cycles are some criteria for stopping the study ; Understanding of physical and mental illness during the study; Married during the study; Relatives death and had surgery during the past two months .)

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, Overweight, swelling of extremities, nausea, bloat). Timepoint: One month, two months, three months after intervention. Method of measurement: Questionnaire.
Secondary Outcome Measures
NameTimeMethod
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.;Reduction in mood symptoms (anxiety and Worry, Restlessness, Nervous tension, Get angry, Snappish, irritableity, depression Withdrawal and irritability and sadness, crying for no reason, feeling alone, Freak out, Behavioral inconsistency). Timepoint: One month, two months, three months after intervention. Method of measurement: Questionnaire.
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