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临床试验/NCT03724656
NCT03724656Unknown不适用

Effects of Intraoperative Stimulation of Acupoints on Postoperative Gastrointestinal Motility Recovery in Patients Undergoing Non-gastrointestinal Abdominal Surgery: A Multicenter Randomized Controlled Trial

Tianjin Nankai Hospital0 个研究点目标入组 600 人开始时间: 2019年3月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
600
主要终点
postoperative venting

研究概览

简要总结

  1. Research name: Effects of intraoperative stimulation of acupoints on postoperative gastrointestinal motility recovery in patients undergoing non-gastrointestinal abdominal surgery.
  2. Research center: Multicenter research
  3. Research design: A randomized controlled study method would be used in this study, in which the investigators would provide electroacupuncture on the basis of general anesthesia for non-gastrointestinal abdominal surgery. The effects of electroacupuncture on postoperative gastrointestinal motility recovery in patients undergoing non-gastrointestinal abdominal surgery will be observed and compared with the control group.
  4. Research population: Patients who are greater or equal to 18 years old and less than 64 years old , meanwhile intend to receive selective/limited non-gastrointestinal surgery under general anesthesia.
  5. Number of participants: 600
  6. Interventions: The treatment group received electroacupuncture intervention 30 minutes before induction of anesthesia. In the treatment group, bilateral Neiguan point, bilateral Zusanli point and bilateral Hegu point were selected, then electroacupuncture was applied and the needle was retained until the end of operation. The control group was treated with non-acupoint shallow acupuncture method. The needle was inserted 5 cm beside the acupoint and the needling depth was less than 2 mm. At the same time, the manual stimulation was avoided, "Deqi" was not obtained, electroacupuncture was applied, electric current was regulated, and the needle was retained until the end of the operation.

详细描述

This study is a large sample, randomized, double-blinded, placebo-controlled and long-term follow-up design. In this study, bilateral Neiguan(PC6), bilateral Zusanli(ST36)and bilateral Hegu (LI4)points were selected for perioperative TAES treatment. accompanied with evaluating the postoperative gastrointestinal motility, the incidence of postoperative nausea and vomiting , as well as the effects on postoperative NRS pain and sleep quality scores . To clarify the effect of TAES on the postoperative spontaneous voiding in patients for laparoscopic surgery is of great significance to the clinical applications and popularization of traditional acupuncture treatment perioperatively across the world.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria
  • Subjects enrolled in this study must accord with all of the following criteria:
  • Age ≥ 18 years old and <64 years old, gender, ethnicity is not limited;
  • It is intended to selective/limited non-gastrointestinal surgery under general anesthesia;
  • Agree to participate in the study and sign an informed consent form;

排除标准

  • Refusing to participate in this study;
  • Patients with cardiac pacemakers and some special groups, such as pregnant women and those who have had many long-term acupuncture treatment experience;
  • Patients with peptic ulcer, perforation or obstruction;
  • Patients with chronic liver and renal dysfunction, and those who use β-blockers or antihypertensive drugs;
  • The attending doctors or researchers believe that there are other unsuitable situations for the study.

研究组 & 干预措施

acupuncture treatment

Experimental

Patients in the TAES treatment group received Transcutaneous Acupoint Electrical Stimulation(TAES) 30 minutes before induction of anesthesia. Bilateral Neiguan(PC6), bilateral Zusanli(ST36)and bilateral Hegu (LI4)point were selected by electroacupuncture stimulation apparatus (HANS G6805-2, Huayi Co, Shanghai, China).After "Deqi", electroacupuncture stimulation apparatus is connected and maintained until the end of operation.

干预措施: acupuncture treatment (Device)

Sham acupuncture treatment

Sham Comparator

The control group was treated with non-acupoint shallow acupuncture method. The needle was inserted 5 cm beside the acupoint and the needling depth was less than 2 mm. At the same time, the manual stimulation and "Deqi" was avoided.

干预措施: sham acupuncture treatment (Device)

结局指标

主要结局

postoperative venting

时间窗: an average of 1 year

Record the time from the end of the procedure to the patient's first venting after operation

次要结局

  • bowel sounds and defecation(an average of 1 year)
  • Biochemical tests(12 months)
  • Postoperative nausea and vomiting(12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jianbo Yu

Department of Anesthesiology, Director, Chief physician, Professor, Doctoral tutor Affiliation: Tianjin Nankai Hospital

Tianjin Nankai Hospital

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