Skip to main content
Clinical Trials/NCT02193477
NCT02193477
Completed
Not Applicable

Effect of Transcutaneous Electrical Acupoint Stimulation (TEAS)on the Incidence Rate of Systemic Inflammatory Response Syndrome (SIRS) in Patients Undergoing Radical Surgery for Gastric Cancer

Air Force Military Medical University, China1 site in 1 country105 target enrollmentJuly 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Systemic Inflammatory Response Syndrome
Sponsor
Air Force Military Medical University, China
Enrollment
105
Locations
1
Primary Endpoint
Incidence rate of SIRS
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to access the effect of Transcutaneous Electrical Acupoint Stimulation(TEAS) on the Incidence rate of Systemic Inflammatory Response Syndrome (SIRS) in patients undergoing radical surgery for gastric cancer

Detailed Description

Patients undergoing elective radical surgery for gastric cancer under general anesthesia were randomly assigned to three groups, control group , TEAS group and sham TEAS group. TEAS group receiving TEAS before general anesthesia induction , 1th day and 2nd day after surgery. TEAS was given through electrodes attached to specific acupoints. The time for TEAS was 30min. Sham TEAS group receiving sham TEAS before general anesthesia induction , 1th day and 2nd day after surgery. Sham TEAS was given through electrodes attached to non-acupoints. The time for sham TEAS was also 30min. Control group were given no TEAS. Incidence rates of SIRS in each group were compared .Venous blood samples from all groups(control group , TEAS group and sham TEAS group) were collected before general anesthesia induction,1th day and 3rd day after surgery. Inflammatory cytokines index including interleukin-6,interleukin-10,Tumor Necrosis Factor- alpha(TNF-α),Interferon-γ(IFN-γ),Monocyte Chemotactic Protein 1(MCP-1),IgG,IgM were measured.

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
January 2015
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Air Force Military Medical University, China
Responsible Party
Principal Investigator
Principal Investigator

QiangWang,MD

associate professor,PhD advisor

Air Force Military Medical University, China

Eligibility Criteria

Inclusion Criteria

  • Age\>30yrs,\<75yrs
  • Scheduled for radical surgery for gastric cancer under general anesthesia;
  • Informed consented

Exclusion Criteria

  • Patients with implanted pacemakers
  • Patients with severe hypertension or cardiac dysfunction;
  • Patients with severe pulmonary disease
  • Patients with hemoglobin\<90g/L

Outcomes

Primary Outcomes

Incidence rate of SIRS

Time Frame: 1st day after surgery

SIRS is defined as 2 or more of the following variables : 1. Fever of more than 38°C (100.4°F) or less than 36°C (96.8°F) 2. Heart rate of more than 90 beats per minute 3. Respiratory rate of more than 20 breaths per minute or arterial carbon dioxide tension (PaCO2) of less than 32mm Hg 4. Abnormal white blood cell count (\>12,000/µL or \< 4,000/µL or \>10% immature granulocyte forms) Incidence rate of SIRS is calculated using the following formula: (Number of SIRS Cases within the group) / (Number of Cases within the group)

Secondary Outcomes

  • Change of Inflammatory cytokines(30 minutes before general anesthesia induction and 1st and 3rd day after the surgery)
  • Incidence rate of SIRS(3rd day after surgery)

Study Sites (1)

Loading locations...

Similar Trials