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Fastigial Nucleus Stimulation for Coronary Heart Disease

A Prospective, Multicenter, Randomized Controlled Trial of Fastigial Nucleus Stimulation in Patients With Coronary Heart Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04121715
Enrollment
200
Registered
2019-10-10
Start date
2019-01-16
Completion date
2022-01-31
Last updated
2019-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Keywords

coronary heart disease, fastigial nucleus stimulation, inflammatory factors

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.

Interventions

DRUGStandard treatment

Refer to the Guidelines for Rational Use of Coronary Heart Diseases.rational selection of antiplatelet drugs, statins, etc. according to the patient's condition

DEVICEFastigial Nucleus Stimulation

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

Sponsors

the Third Hospital of Mianyang
CollaboratorUNKNOWN
Affiliated Hospital of North Sichuan Medical College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Observe the changes of pNN50(Percentage of the difference between adjacent RR intervals >50ms ) after treatment.baseline,1monthObserve the changes of pNN50(%)after treatment in the two groups of patients.
Observe the changes of serum IL-6 after treatment.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve 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.baseline,1monthObserve the changes of rMSSD(ms)after treatment in the two groups of patients.

Secondary

MeasureTime frameDescription
Follow-up rate of major cardiovascular events12monthsThe 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.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026