ClinicalTrials.Veeva

Menu

TEAS Enhanced Recovery After Laparoscopic Colon Surgery (ARCO)

Z

Zhihong LU

Status

Completed

Conditions

Postoperative Recovery

Treatments

Other: TEAS
Other: false stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT02921529
XJH-A-2016-09-01

Details and patient eligibility

About

The purpose of this study is to observe the effects of transcutaneous electrical acupoint stimulation(TEAS) on postoperative recovery after laparoscopic colon surgery.

Full description

Patients were randomly assigned to two groups, receiving TEAS andno stimulation respectively. Interventions were given 30min before anesthesia and 1, 2 , 3 day after surgery, lasted 30min each time . The acupoints of TEAS group are bilateral ST36/SP6 combined with PC6/LI4, and the control group only attach electrodes without electric current. The frequency of TEAS is set to 2/10 Hz. After surgery, the time of meeting discharge criteria, first flatus and defecation were recorded. Score of PONV, life quality, sleep quality and VAS of pain were evaluated 24, 48 and 72h after surgery. The postoperative complications, re-exploration, cost of hospitalization and adverse events were also recorded.

Enrollment

100 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age between 18 to 75 years old;
  • ASA I-III;
  • Scheduled for elective laparoscopic colon surgery under general anesthesia;
  • BMI between 18 and 30;
  • Informed consented.

Exclusion criteria

  • Patients with contraindications to the use of electroacupuncture, such as skin damage or infection at the acupoints;
  • Patients with difficulty in communication;
  • Emergency surgery;
  • Patients who are with distant metastasis;
  • Patients who are with history of myocardial infarction or cerebral infarction in the past six months;
  • Patients who are with long history of taking NSAIDS,hormone or immunosuppressive agents;
  • Patients who are recruited in other clinical trials in the last 3 months;
  • Other situations researcher think shouldn't be included.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

100 participants in 2 patient groups

TEAS
Experimental group
Description:
Patients were given 30min of TEAS(transcutaneous electrical acupoint stimulation) before anesthesia and 1,2,3 day after surgery
Treatment:
Other: TEAS
false stimulation
Sham Comparator group
Description:
Attach electrodes without electric current
Treatment:
Other: false stimulation

Trial contacts and locations

3

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems