跳至主要内容
临床试验/KCT0009149
KCT0009149招募中Unknown

Efficacy and safety of acupuncture for blood pressure fluctuation during total laparoscopic hysterectomy: a randomized controlled, parallel-grouped pilot study

CHA University Ilsan Medical Center0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方
入组人数
30

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
19(Year) 至 69(Year)(—)
性别
Female

入选标准

  • between age of 19 and 69,
  • American Society of Anesthesiologists (ASA) class I or II,
  • required surgical removal of uterus by a gynecology specialist,
  • scheduled to have total laparoscopic hysterectomy in advance.
  • agree to participate in clinical trials and providing signed informed consent

排除标准

  • expected survival within 3 months,
  • emergency operation which was not scheduled in advance,
  • hypertension or hypotension that can significantly interfere with the study result,
  • diagnosis of arrhythmia, such as atrial fibrillation, frequent ventricular or supraventricular premature beats,
  • diagnosis of heart failure or valvular disease,
  • anemia of hemoglobin < 12 g/dL,
  • incapable of surgery due to hemodynamic or medical reasons other than stated above,
  • incapable of receiving acupuncture treatment on determined location,
  • current use of gonadotropin-releasing hormone receptor agonists,
  • current use of drugs that may interfere with the result, including steroids, immunosuppressants, and psychiatric disorders,
  • significant comorbidities that may interfere with the interpretation of intervention efficacy or results, such as stroke, myocardial infarction, kidney disease, dementia, or epilepsy,
  • pregnant, planning to be pregnant within study period, or breastfeeding,
  • previous participation in any other clinical trial within 1 month of participation, planning to participate another clinical trial within 6 months after enrollment date, or planning to participate another clinical trial on follow-up period,
  • fail to write the informed consent form voluntarily,
  • being deemed to be unsuitable for participation.

研究者

发起方
CHA University Ilsan Medical Center

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