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临床试验/KCT0001929
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

发起方
Dong-Eui University Oriental Medicine Hospital

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