KCT0001929已完成未知
A clinical study on menstrual pain investigating the effectiveness of an integrated diagnostic system combining typology, complexion, pulse, and symptoms
Dong-Eui University Oriental Medicine Hospital0 个研究点目标入组 1,026 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,026
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 18(Year) 至 o Limit(—)
- 性别
- Female
入选标准
- •?Experimental group
- •Females aged 18 or above
- •Menstrual cycle length of 21–39 days
- •Discomfort in daily life or interpersonal activities from menstrual pain
- •Score of 4 or above on MMP (Measure of Menstrual Pain)19
- •? Control group
- •Female aged 18 or above
- •Menstrual cycle length of 21–39 days
- •Little or no discomfort in daily life or interpersonal activities from menstrual pain
- •Score of 3 or below on MMP (Measure of Menstrual Pain)19
排除标准
- •Menstrual cycle length of less than 20 days or more than 40 days
- •Premenopausal symptoms (irregular menstruation, rosacea)
- •Polycystic Ovarian Syndrome
- •Sterility
- •Cancer history within the previous 5 years
- •Severe diseases with the potential to affect signs and symptoms
- •- Cardiovascular disease, renal disease, diabetes, anemia
- •- Hypertensive patients unable to adjust blood pressure
- •- Active liver disease or gallbladder disease
- •- Hyper- or hypothyroidism
- •- Psychiatric disorders or on antidepressants
- •- Sanhupung (postpartum syndrome) or musculoskeletal diseases above moderate level
- •Otherwise assessed by the investigators to be either mentally or physically unsuitable to participate in the study
研究者
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