IRCT20220720055514N1招募中2 期
Comparison of the effect of Vitagnus capsules, Soy and the combination of Vitagnus and Soy in students with premenstrual syndrome
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 108
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 16 years 至 45 years(—)
- 性别
- Female
入选标准
- •Be a student living in the dormitory of Mashhad University of Medical Sciences
- •Have written and informed consent to participate in the study
- •Be of Iranian and Muslim nationality
- •Be 16-45 years old
- •Have regular menstruation with menstrual intervals of 21-38 days and a bleeding period of less than 7 days
- •Have a BMI less than 30 kg/m2
- •Have 5 or more than 5 symptoms out of 11 symptoms of the premenstrual syndrome temporary diagnosis form and at least one of the first 4 symptoms of the questionnaire
- •Do not suffer from physical or mental illness
- •Do not suffer from severe Depression, Stress and Anxiety according to DASS 21 form
- •Not taking any special medicine
- •She has not taken effective drugs (chemical or herbal) on premenstrual syndrome in the last three months
- •Has not experienced an unfortunate accident in the last 6 months
- •Not a professional athlete
- •Do not follow a special diet or vegetarian diet
- •Not allergic to Vitagnus and Soy products
- •No history of breast cancer in first degree relatives
- •Do not consume Alcohol, Cigarettes or any drugs
排除标准
- •Get married while studying
- •Complications or allergies to Vitagnus medicine, Soy, or the combination of Vitagnus and Soy occur
- •Experienced any unfortunate incident while studying
- •Suffer physical and mental illness while studying
- •Do not use any type of treatment to relieve symptoms of PMS during the study period
- •Do not complete the daily symptom registration questionnaire or complete the form incompletely
- •Do not use the medicine according to the instructions and opinion of the pharmacologist
- •Do not want to continue taking medicine and cooperate in the plan
研究者
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