跳至主要内容
临床试验/ITMCTR2100005394
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

发起方
The First Affiliated Hospital ,University of South China

相似试验