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Fastigial Nucleus Stimulation for Coronary Heart Disease

Primary Purpose

Coronary Disease

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Fastigial Nucleus Stimulation
Standard treatment
Sponsored by
Affiliated Hospital of North Sichuan Medical College
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Disease focused on measuring coronary heart disease, fastigial nucleus stimulation, inflammatory factors

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Coronary angiography was performed after admission, and coronary heart disease was diagnosed (coronary angiography showed at least one coronary artery with a diameter reduction of ≥50% from more than two different angles)
  • Patients and their families agreed and signed informed consent

Exclusion Criteria:

  • Severe chronic heart failure, and LVEF <30%
  • Body temperature > 38 ° C and / or combined with severe infection in any system
  • Severe liver and kidney dysfunction
  • Malignant tumor
  • Autoimmune diseases
  • High blood pressure and diabetes with severe comorbidities
  • Use of implantable electronic devices
  • Intracranial implanted vascular stents
  • Surface treatment electrode conductive materials Allergic or mastoid skin lesions

Sites / Locations

  • The Third Hospital of Mianyang

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

standard medication

standard medication+fastigial nucleus stimulation

Arm Description

standard medication:Refer to the "Guidelines for Rational Use of Coronary Heart Diseases"

fastigial nucleus stimulation:Use fastigial nucleus stimulation therapy device (Shanghai Renhe Medical Equipment Co., Ltd. CVFT series), each stimulation for 30 min, once a day, each patient treatment for about 20 days. standard medication:Refer to the "Guidelines for Rational Use of Coronary Heart Diseases"

Outcomes

Primary Outcome Measures

Observe the changes of serum IL-6 after treatment.
Observe the changes of serum IL-6 levels(pg/ml)after treatment in the two groups of patients.
Observe the changes of serum hs-CRP after treatment.
Observe the changes of serum hs-CRP levels(mg/l)after treatment in the two groups of patients.
Observe the changes of serum TNF-α after treatment.
Observe the changes of serum TNF-α levels(pg/ml)after treatment in the two groups of patients.
Observe the changes of serum Lp-PLA2 after treatment.
Observe the changes of serum Lp-PLA2 levels(ng/ml)after treatment in the two groups of patients.
Observe the changes of serum SOD(Superoxide dismutase) after treatment.
Observe the changes of serum SOD levels(ng/ml)after treatment in the two groups of patients.
Observe the changes of serum GPX(Glutathione peroxidase) after treatment.
Observe the changes of serum GPX levels(ng/ml)after treatment in the two groups of patients.
Observe the changes of serum MDA(Malondialdehyde) after treatment.
Observe the changes of serum MDA levels(nmol/ml)after treatment in the two groups of patients.
Observe the changes of serum AOPP(Advanced oxidation protein product) after treatment.
Observe the changes of serum AOPP levels(umol/l)after treatment in the two groups of patients.
Observe the changes of SDNN(Standard Deviation of the NN intervals) after treatment.
Observe the changes of SDNN(ms)after treatment in the two groups of patients.
Observe the changes of SDANN(Standard Deviation of mean NN intervals in 5-minute recordings) after treatment.
Observe the changes of SDANN(ms)after treatment in the two groups of patients.
Observe the changes of SDNN In(Average of the standard deviation of the NN interval every 5 minutes) after treatment.
Observe the changes of SDNN In(ms)after treatment in the two groups of patients.
Observe the changes of rMSSD(square root of the mean squared differences of successive NN intervals) after treatment.
Observe the changes of rMSSD(ms)after treatment in the two groups of patients.
Observe the changes of pNN50(Percentage of the difference between adjacent RR intervals >50ms ) after treatment.
Observe the changes of pNN50(%)after treatment in the two groups of patients.

Secondary Outcome Measures

Follow-up rate of major cardiovascular events
The improvement of symptoms and the in-stent restenosis, myocardial infarction, readmission due to heart failure, and mortality were observed in the two groups after 12 months of discharge.

Full Information

First Posted
September 25, 2019
Last Updated
October 8, 2019
Sponsor
Affiliated Hospital of North Sichuan Medical College
Collaborators
the Third Hospital of Mianyang
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1. Study Identification

Unique Protocol Identification Number
NCT04121715
Brief Title
Fastigial Nucleus Stimulation for Coronary Heart Disease
Official Title
A Prospective, Multicenter, Randomized Controlled Trial of Fastigial Nucleus Stimulation in Patients With Coronary Heart Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 16, 2019 (Actual)
Primary Completion Date
January 2021 (Anticipated)
Study Completion Date
January 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Affiliated Hospital of North Sichuan Medical College
Collaborators
the Third Hospital of Mianyang

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To observe the effects of fastigial nucleus stimulation on serum inflammation, oxidative stress related factors, cardiac autonomic function and prognosis in patients with coronary heart disease
Detailed Description
In recent years, with the improvement of the material living standards of the investigators residents and the change of working lifestyle, the prevalence and mortality of coronary heart disease (CHD) in urban and rural residents in China have increased year by year. According to statistics, the number of patients with coronary heart disease in China is currently 11 million. Coronary heart disease has become a major health problem in China. At present, it is found that inflammatory reaction and oxidative stress factors are involved in the occurrence and development of coronary heart disease, and their indicators such as heart rate variability are related to the prognosis of coronary heart disease. Fastigial nucleus stimulation (FNS) has been widely used in the treatment of various diseases such as cerebrovascular disease, migraine, and eye diseases. The study found that FNS can reduce inflammatory cytokines and oxidative stress factors in ischemic myocardium and improve heart rate variability in rats with myocardial infarction. The aim of this study was to investigate whether FNS can improve the aforementioned indicators and clinical outcomes in patients with coronary heart disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Disease
Keywords
coronary heart disease, fastigial nucleus stimulation, inflammatory factors

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
standard medication
Arm Type
Active Comparator
Arm Description
standard medication:Refer to the "Guidelines for Rational Use of Coronary Heart Diseases"
Arm Title
standard medication+fastigial nucleus stimulation
Arm Type
Experimental
Arm Description
fastigial nucleus stimulation:Use fastigial nucleus stimulation therapy device (Shanghai Renhe Medical Equipment Co., Ltd. CVFT series), each stimulation for 30 min, once a day, each patient treatment for about 20 days. standard medication:Refer to the "Guidelines for Rational Use of Coronary Heart Diseases"
Intervention Type
Device
Intervention Name(s)
Fastigial Nucleus Stimulation
Other Intervention Name(s)
Standard treatment
Intervention Description
Select mode 3, frequency 136, intensity below 90, ratio 1.0-2.0, based on the patient's no discomfort. The main pole is attached to the bilateral mastoid, and the auxiliary pole is attached to the bilateral internal cave. Non-invasive introduction of bio-electricity into the cerebellar nucleus for stimulation
Intervention Type
Drug
Intervention Name(s)
Standard treatment
Intervention Description
Refer to the "Guidelines for Rational Use of Coronary Heart Diseases".rational selection of antiplatelet drugs, statins, etc. according to the patient's condition
Primary Outcome Measure Information:
Title
Observe the changes of serum IL-6 after treatment.
Description
Observe the changes of serum IL-6 levels(pg/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum hs-CRP after treatment.
Description
Observe the changes of serum hs-CRP levels(mg/l)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum TNF-α after treatment.
Description
Observe the changes of serum TNF-α levels(pg/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum Lp-PLA2 after treatment.
Description
Observe the changes of serum Lp-PLA2 levels(ng/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum SOD(Superoxide dismutase) after treatment.
Description
Observe the changes of serum SOD levels(ng/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum GPX(Glutathione peroxidase) after treatment.
Description
Observe the changes of serum GPX levels(ng/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum MDA(Malondialdehyde) after treatment.
Description
Observe the changes of serum MDA levels(nmol/ml)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of serum AOPP(Advanced oxidation protein product) after treatment.
Description
Observe the changes of serum AOPP levels(umol/l)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of SDNN(Standard Deviation of the NN intervals) after treatment.
Description
Observe the changes of SDNN(ms)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of SDANN(Standard Deviation of mean NN intervals in 5-minute recordings) after treatment.
Description
Observe the changes of SDANN(ms)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of SDNN In(Average of the standard deviation of the NN interval every 5 minutes) after treatment.
Description
Observe the changes of SDNN In(ms)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of rMSSD(square root of the mean squared differences of successive NN intervals) after treatment.
Description
Observe the changes of rMSSD(ms)after treatment in the two groups of patients.
Time Frame
baseline,1month
Title
Observe the changes of pNN50(Percentage of the difference between adjacent RR intervals >50ms ) after treatment.
Description
Observe the changes of pNN50(%)after treatment in the two groups of patients.
Time Frame
baseline,1month
Secondary Outcome Measure Information:
Title
Follow-up rate of major cardiovascular events
Description
The improvement of symptoms and the in-stent restenosis, myocardial infarction, readmission due to heart failure, and mortality were observed in the two groups after 12 months of discharge.
Time Frame
12months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Coronary angiography was performed after admission, and coronary heart disease was diagnosed (coronary angiography showed at least one coronary artery with a diameter reduction of ≥50% from more than two different angles) Patients and their families agreed and signed informed consent Exclusion Criteria: Severe chronic heart failure, and LVEF <30% Body temperature > 38 ° C and / or combined with severe infection in any system Severe liver and kidney dysfunction Malignant tumor Autoimmune diseases High blood pressure and diabetes with severe comorbidities Use of implantable electronic devices Intracranial implanted vascular stents Surface treatment electrode conductive materials Allergic or mastoid skin lesions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Runfeng Zhang, Ph.D
Organizational Affiliation
the Third Hospital of Mianyang
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Wensong Li, master
Organizational Affiliation
the Third Hospital of Mianyang
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xin Lei, master
Organizational Affiliation
Affiliated Hospital of North Sichuan Medical College
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xiaoju Liu, master
Organizational Affiliation
Affiliated Hospital of North Sichuan Medical College
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Third Hospital of Mianyang
City
Mianyang
State/Province
Sichuan
ZIP/Postal Code
0816
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
De-identified individual participant data for all primary and secondary outcome measures will be made available
IPD Sharing Time Frame
Data will be available within 6months of study completion
IPD Sharing Access Criteria
Data access requests will be reviewed by an external independent Reviwe Panel.Requestors will be required to sign a Data Access Agreement
IPD Sharing URL
http://bethesda.org

Learn more about this trial

Fastigial Nucleus Stimulation for Coronary Heart Disease

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