跳至主要内容
临床试验/NCT03222557
NCT03222557Unknown不适用

Electroacupuncture for Postoperative Ileus After Laparoscopic Surgery for Mid and Low Rectal Cancer: A Prospective, Randomized, Sham-controlled Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 164 人开始时间: 2017年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
164
试验地点
1
主要终点
GI-2 recovery

研究概览

简要总结

This is a prospective, randomized, sham-controlled, superiority trial that aimed to investigate the efficacy of electroacupuncture (EA) in reducing the duration of postoperative ileus and hospital stay after laparoscopic total mesorectal excision or abdominoperineal resection for rectal cancer.

详细描述

Background: Postoperative ileus (POI) remains a significant problem after colorectal surgery that adversely influences patients' recovery and prolongs hospital stay. The investigators' previous study demonstrated that electroacupuncture (EA) at Zusanli, Sanyinjiao, Hegu, and Zhigou reduces the duration of POI and hospital stay after laparoscopic resection of colonic and upper rectal cancer (Ng et al. Gastroenterology 2013; 144: 307-313). However, patients with mid/low rectal cancer undergoing laparoscopic sphincter-preserving total mesorectal excision (TME) or abdominoperineal resection (APR) were excluded. These complicated cases are apparently more likely to develop prolonged ileus and morbidity after surgery.

Objectives: To investigate the efficacy of EA in reducing the duration of POI and hospital stay after laparoscopic TME or APR for rectal cancer.

Hypothesis: Rectal cancer patients undergoing laparoscopic TME or APR within a fast-track perioperative program who receive EA will have shorter duration of POI and hospital stay when compared with those who receive sham acupuncture (SA).

Design: Prospective, randomized, sham-controlled, superiority trial.

Subjects: One hundred and sixty four consecutive patients with mid/low rectal cancer undergoing laparoscopic surgery without the need of conversion will be recruited. All patients will follow a standard perioperative fast-track program.

研究设计

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

盲法说明

The acupuncturist is the only individual who is aware of the treatment allocation; the patients randomized to the EA/SA groups and the outcome assessor are blinded to the treatment allocation.

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Consecutive patients (aged between 18 and 80) with mid/low rectal cancer (adenocarcinoma in the rectum of which the lowest margin of the tumor is located within 12 cm of the anal verge as measured by rigid sigmoidoscopy) undergoing laparoscopic sphincter-preserving TME or APR without the need of conversion
  • •American Society of Anesthesiologists grading I-III
  • •Informed consent available

排除标准

  • •Patients with previous experience of acupuncture
  • •Those undergoing simultaneous laparoscopic resection of rectal cancer and other coexisting intraabdominal diseases
  • •Those undergoing laparoscopic resection of rectal cancer with en bloc resection of surrounding organs
  • •Those who developed intraoperative problems or complications (e.g. bleeding, tumor perforation) that required conversion
  • •Those undergoing emergency surgery
  • •Those with previous history of midline laparotomy
  • •Those with evidence of peritoneal carcinomatosis
  • •Those who are expected to receive epidural anesthesia or analgesia
  • •Those with cardiac pacemaker
  • •Those who are pregnant
  • •Those who are allergic to the acupuncture needles

研究组 & 干预措施

Electroacupuncture (EA)

Experimental

Bilateral acupoints relevant to the treatment of abdominal pain, abdominal distension, and constipation, including Zusanli (stomach meridian ST-36), Sanyinjiao (spleen meridian SP-6), Hegu (large intestine meridian LI-4), and Zhigou (triple energizer meridian TE-6), will be used. Electric stimulation at a frequency of 50 Hz will be employed to the needles

干预措施: Electroacupuncture (Procedure)

Electroacupuncture (EA)

Experimental

Bilateral acupoints relevant to the treatment of abdominal pain, abdominal distension, and constipation, including Zusanli (stomach meridian ST-36), Sanyinjiao (spleen meridian SP-6), Hegu (large intestine meridian LI-4), and Zhigou (triple energizer meridian TE-6), will be used. Electric stimulation at a frequency of 50 Hz will be employed to the needles

干预措施: Electroacupuncture (Device)

Sham Acupuncture (SA)

Sham Comparator

Sterile blunt-tip needles will be placed (without skin penetration) 20 mm away from the acupoints. The needle will be first inserted through a sterile plastic tube mounted on a foam block, and then pressed on the skin. The foam block compresses to give the impression that the needle is penetrating the skin, thus providing a SA effect. 'Pseudostimulation' will be given by deliberately connecting the needle to the incorrect output socket of the electroacupuncture device, thus there will be no flow of electric current.

干预措施: Sham Acupuncture (Procedure)

Sham Acupuncture (SA)

Sham Comparator

Sterile blunt-tip needles will be placed (without skin penetration) 20 mm away from the acupoints. The needle will be first inserted through a sterile plastic tube mounted on a foam block, and then pressed on the skin. The foam block compresses to give the impression that the needle is penetrating the skin, thus providing a SA effect. 'Pseudostimulation' will be given by deliberately connecting the needle to the incorrect output socket of the electroacupuncture device, thus there will be no flow of electric current.

干预措施: Sham Acupuncture (Device)

结局指标

主要结局

GI-2 recovery

时间窗: Up to 10 days

A composite assessment that measured upper (first tolerance of solid food) and lower (first bowel movement) GI tract recovery, with time to achieve GI-2 recovery based on the last event to occur

次要结局

  • Pain scores on the first 3 postoperative days(Up to postoperative day 3)
  • Postoperative analgesic requirement(Up to 1 month)
  • Short-term morbidity(Up to 1 month)
  • Adverse events related to EA/SA(Up to 1 month)
  • Time of first passing flatus(Up to 10 days)
  • Length of hospital stay(Up to 1 month)

研究者

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

Simon S. M. Ng

Professor of Surgery

Chinese University of Hong Kong

研究点 (1)

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