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Clinical Trials/NCT02239159
NCT02239159
Completed
Not Applicable

Acupuncture-assisted-anesthesia to Improve Complications After Digestive Surgery in Elderly Patients:Multi-center Double-blinded Randomized Controlled Trial

Air Force Military Medical University, China1 site in 1 country748 target enrollmentApril 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Complications
Sponsor
Air Force Military Medical University, China
Enrollment
748
Locations
1
Primary Endpoint
Number of Participants with Pulmonary Adverse Events as a Measure of Morbidity Tolerability
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The investigators assume that transcutaneous electric acupoint stimulation (TEAS) pretreatment may activate the endogenous protective mechanism, as a result protect the patients against subsequent surgical stress pregnancy. And TEAS may induce the production of endogenous analgesic transmitters, so develop an anesthetic-sparing effect. The investigators believe this intervention will reduce the subsequent incidence, duration and severity of organ dysfunction, possibly reducing the morbidity, even mortality. So in this study, the investigators hypothesize that TEAS before anesthesia and during surgery would decrease the morbidity and mortality of postoperative complications in 30 days after digestive surgery in elderly patients .

Detailed Description

Patients older than 65 years old are at higher risk of postoperative morbidity and mortality. With the increasing number of old patients scheduled for digestive surgery, exploring methods to decrease postoperative morbidity is very important. Noninvasive methods may be easier to clinically use. Transcutaneous electric acupoint stimulation (TEAS)has been proved to decrease need for general anesthetics during anesthesia, and to alleviate systemic inflammatory response. Considering the morbidity and mortality after surgery is closely related to use of anesthetics and inflammatory response,TEAS may be a good selection for improving postoperative outcomes.Among the postoperative complications, pulmonary complication and systemic inflammatory response syndrome is with higher incidence, so we will focus on these two complications in our study.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
October 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

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

Zhihong LU

Dr.

Air Force Military Medical University, China

Eligibility Criteria

Inclusion Criteria

  • Provide written informed consent
  • Age ≥65 years of age
  • Elective digestive surgery under general anesthesia

Exclusion Criteria

  • ASA(American Society of Anesthesiologists) status\> Ⅲ
  • Patients undergoing surgery within 12 h of admission to hospital
  • Patients undergoing surgery of the chest
  • Patients suffered from neurologic disorder or impaired mental state
  • Patients with contraindications to the use of electro-acupuncture, such as skin damage or infection at the acupoints
  • Patients with experience of transcutaneous electrical stimulation treatment

Outcomes

Primary Outcomes

Number of Participants with Pulmonary Adverse Events as a Measure of Morbidity Tolerability

Time Frame: participants will be followed from the end of the surgery to 30 days after surgery

Secondary Outcomes

  • Number of participants died of all causes(Participants will be followed from the end of the surgery to 30 days after surgery)
  • Number of participants with Systemic Inflammatory Response Syndrome(SIRS)(Participants will be followed from the end of the surgery to 30 days after surgery)
  • Number of participants with ICU admission(participants will be followed for the duration of hospital stay after surgery, an expected average of 7 days)
  • Length of ICU stay(participants will be followed for the duration of hospital stay after surgery, an expected average of 7 days)
  • Length of hospital stay(participants will be followed for the duration of hospital stay after surgery, an expected average of 7days)

Study Sites (1)

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