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Neuroprotective Study of Electroacupuncture Pretreatment in Patients Undergoing Cardiac Surgery

Primary Purpose

Stroke, Brain Injuries

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
non electroacupuncture stimulation
Electroacupuncture pretreatment
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stroke focused on measuring brain protection, cardiac surgery, heart valve replacement, electroacupuncture, pretreatment, preconditioning, Thoracic Surgery

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

This study enrolls a group of 40-65years patients who have heart valve disease who need valve replacement.

Inclusion Criteria:

  • patients who have the indication for aortic or mitral valve replacement
  • patients would like to accept the follow-up and sign the informed consent
  • patients with heart function of NYHA I-III degree.

Exclusion Criteria:

  • pregnant or nursing women
  • comorbid with coronary artery disease
  • patients with heart function of NYHA IV degree
  • renal dysfunction with serum creatinine level>or=2mg/dl(177umol/L)
  • anticipated life span < 12 months
  • enrollment in other clinical trials at the same time not reaching the primary endpoint and probably interference the present trial.

Sites / Locations

  • Xijing Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Electroacupuncture

Control

Arm Description

Outcomes

Primary Outcome Measures

Cerebrovascular complications and Score of neurological defect

Secondary Outcome Measures

The S-100B and NSE blood level

Full Information

First Posted
November 22, 2009
Last Updated
June 23, 2015
Sponsor
Xijing Hospital
Collaborators
Air Force Military Medical University, China
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1. Study Identification

Unique Protocol Identification Number
NCT01020266
Brief Title
Neuroprotective Study of Electroacupuncture Pretreatment in Patients Undergoing Cardiac Surgery
Official Title
Clinical Trial of Cerebral Protective Effects of Repeated Electroacupuncture Pretreatment in Heart Valve Replacement Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
November 2009
Overall Recruitment Status
Completed
Study Start Date
December 2009 (undefined)
Primary Completion Date
September 2010 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xijing Hospital
Collaborators
Air Force Military Medical University, China

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the neuroprotective effect of electroacupuncture pretreatment in patients undergoing cardiac surgery as an preventive sequela in a randomized and controlled clinical trial. In addition, to investigate the role of inflammatory responses in the precess of the protection.
Detailed Description
Heart valve replacement surgery has been proved to be an effective method in treating both regenerative and rheumatic valve disease. Current studies showed that cardiopulmonary bypass (CPB) and operation related cerebral injury is associated with worse patient morbidity and mortality after elective valve replacement surgery. Recently, Electroacupuncture (EA) pretreatment was proved to produced cerebral protective effects by mimicking ischemic preconditioning in animal models. However, the evidence that EA pretreatment can improve the clinical outcomes such as mortality and morbidity, is still lacking. The investigators perform a randomized controlled study to evaluate that EA pretreatment can improve the outcomes of cardiac surgery. Purpose: The purpose of this study is to examine if EA pretreatment can decrease the mortality and postoperative cerebrovascular complications in patients undergoing cardiac surgery. The effect will be assessed by mortality, scores of neurological defect, post operative cognitive dysfunction and stroke. Methods: Study patients will be randomized to cardiac surgery with EA pretreatment or conventional cardiac surgery in the Department of cardiovascular surgery, Xijing Hospital. EA pretreatment is performed at Baihui acupoint 30 min per day 5 consecutive days before the heart valve replacement surgery.Primary study outcome is cerebrovascular complications within 6 postoperative months. Secondary outcomes include the S-100B and NSE blood level measured during the first 72 hours of surgery follow-up, the several cytokines, including TNF-a, IL-8, IL-6, IL-10 and HMGB-1 blood level measured during the first 7 days of surgery follow-up, all cardiovascular haemodynamic parameters as measured by a pulmonary artery catheter, the length of intensive care unit (ICU) stay and length of postoperative hospital stay.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Brain Injuries
Keywords
brain protection, cardiac surgery, heart valve replacement, electroacupuncture, pretreatment, preconditioning, Thoracic Surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Electroacupuncture
Arm Type
Active Comparator
Arm Title
Control
Arm Type
Sham Comparator
Intervention Type
Procedure
Intervention Name(s)
non electroacupuncture stimulation
Intervention Description
The same procedure as electroacupuncture except stimulation
Intervention Type
Procedure
Intervention Name(s)
Electroacupuncture pretreatment
Other Intervention Name(s)
Acupuncture, preconditioning, electric stimulation
Intervention Description
According to the theory of traditional Chinese medicine, Baihui(GV20) acupoint was chosen and the acupuncture points were identified according to traditional anatomical localization. Once insertion was made at the acupuncture point, the needle was stimulated electrically with the intensity of 0.8-1.9 mA and frequency of 5/30 Hz for 30 min per day using an Electronic Acupuncture Treatment Instrument for 5 consecutive days before the heart valve replacement surgery.
Primary Outcome Measure Information:
Title
Cerebrovascular complications and Score of neurological defect
Time Frame
before treatment, after the first treatment, 7, 28days after treatment and follow up at 6 months after treatment
Secondary Outcome Measure Information:
Title
The S-100B and NSE blood level
Time Frame
before treatment, after the last treatment, before surgery, and the first 72 hours of surgery follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
This study enrolls a group of 40-65years patients who have heart valve disease who need valve replacement. Inclusion Criteria: patients who have the indication for aortic or mitral valve replacement patients would like to accept the follow-up and sign the informed consent patients with heart function of NYHA I-III degree. Exclusion Criteria: pregnant or nursing women comorbid with coronary artery disease patients with heart function of NYHA IV degree renal dysfunction with serum creatinine level>or=2mg/dl(177umol/L) anticipated life span < 12 months enrollment in other clinical trials at the same time not reaching the primary endpoint and probably interference the present trial.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aideng Weng, Ph.D.
Organizational Affiliation
Xijing Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Xijing Hospital
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China

12. IPD Sharing Statement

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Neuroprotective Study of Electroacupuncture Pretreatment in Patients Undergoing Cardiac Surgery

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