ITMCTR2100005394尚未招募未知
Multiple-center randomized controlled clinical study of electroacupuncture relieving primary dysmenorrhea
The First Affiliated Hospital ,University of South China0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 性别
- Female
入选标准
- •(1) Meet the diagnostic criteria of primary dysmenorrhea
- •(2) Age ranged from 14 to 35 years old.
- •(3) Basic rules of the menstrual cycle (28 ±, 7 days).
- •(4) Designers who volunteered to participate in the clinical study signed an informed consent, did not have other treatment for dysmenorrhea within 1 month before the acupuncture treatment, and did not take NSAoidal anti-inflammatory drugs and painkillers within the first 2 weeks of the electric needle.
- •(5) Willing to cooperate with the treatment operation, examination and efficacy evaluation, and did not participate in other clinical experiments.
- •(6) Average pain visual simulation score (VisualAnalogueScale, VAS) for 4cm.
- •(7) Sign the informed consent form.
- •The above 7 simultaneous applicants can only be included in the test.
排除标准
- •(1) After examination, western medicine is diagnosed as a secondary dysmenorrhea caused by uterine fibroids, adenomysiosis, endometriosis, pelvic inflammation, internal foreign body, ovarian lesions and other organic lesions.
- •(2) Menstrual period is successively irregular.
- •(3) Patients with serious cardiovascular and cerebrovascular diseases, serious diabetes mellitus, serious infection, liver and renal insufficiency, hematopoietic diseases, AIDS, and tuberculosis, hepatitis and other infectious diseases.
- •(4) People with obvious mental illness and obvious cognitive dysfunction.
- •(5) Pregnancy or pregnancy, lactation and postpartum within 1 year.
- •(6) Those who are participating in other clinical trials.
- •Note: Studies were excluded for any one of the above compliance
研究者
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