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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04383080
Other study ID # NYMUH IRB No.2019b007
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date December 17, 2022

Study information

Verified date October 2022
Source National Yang Ming Chiao Tung University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The advantages of laser acupuncture are a non-invasive, painless, low risk of infection and high safety. Laser acupuncture as a treatment tool has the following advantages1.Painless, 2. Non-invasive treatment, the subject is highly accepted, the risk of infection and needle stick is low, 3. Very few side effects such as fainting, bleeding, 4. The therapeutic dose is easy to operate, and the instrument output frequency, power and time can be controlled. Through the clinical physiological function test plus the verification and analysis of the quantitative test values, it will be more able to define the new role of laser acupuncture treatment in patients with heart failure from the perspective of Chinese medicine.


Description:

From the perspective of ancient books, the discussion of heart failure in the etiology and pathogenesis of traditional Chinese medicine was first seen in the "Shu Wen". It is clearly pointed out that "heart qi" is the basic pathogenesis of heart failure. The "qi" and "blood" of Chinese medicine are closely related. The blood line is driven by the gas, the blood is bloody, and the qi deficiency is unable to push the blood to blood. If the qi deficiency, it would lead to blood stasis; There were studies have indicated that traditional acupuncture treatment can increase exercise tolerance and adjust autonomic nerve activity in patients with chronic heart failure, and can reduce their readmission rate and mortality rate in patients with acute heart failure. Studies using laser acupuncture to treat patients with heart failure have also found that they can increase the subject's six-minute walking distance.


Recruitment information / eligibility

Status Completed
Enrollment 17
Est. completion date December 17, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - Age over 20 years of age, with written informed consent. - NYHA:stage II-III. - All patients had LVEF <40% caused by dilated or ischemic cardiomyopathy. - Acute HF patient presenting with dyspnea related to cardiogenic pulmonary edema. - All patients had sinus rhythm, were stable and compensated with individually optimized standard heart failure medication as well as oral anticoagulants for at least 3 months before (including prophylactic defibrillator placement). - Systolic blood pressure > 95 mmHg at admission. - B-type natriuretic peptide (BNP) > 150 pg/mL or NT-pro BNP > 600 pg/mL. Exclusion Criteria: - Age under 20. - Major cardiovascular events and treatments occurred four weeks before hospitalization. - Major cardiovascular surgery or treatment will be performed in the next 6 months. - Pregnant or expected to pregnancy within a year. - Require a heart transplant in 6 months. - Uncontrolled atrial or ventricular dysrhythmias. - Uncompensated congestive heart failure. - Heart failure due to congenital heart disease or obstructive myocardial disease

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture
acupuncture at specific acupuncture points
Device:
Low-level laser therapy
low level laser emission on specific acupuncture points

Locations

Country Name City State
Taiwan National Yang Ming University Hospital Ilan

Sponsors (1)

Lead Sponsor Collaborator
National Yang Ming Chiao Tung University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other Questionnaires_Instrumental activities of daily living (IADL);Scoring from 0 to 4 and higher scores mean better outcome. At the 4th, 12t, 20th and 24th week
Other Questionnaires_EuroQol- 5 Dimension (EQ-5D);Scoring from 1 to 3 and higher scores mean better outcome. At the 4th, 12t, 20th and 24th week
Other Questionnaires_The Minnesota LIVING WITH HEART FAILURE® Questionnaire (MLHFQ);Scoring from 0 to 5 and higher scores mean better outcome. At the 4th, 12t, 20th and 24th week
Other Questionnaires_Patient Health Questionnaire-9 (PHQ-9);Scoring from 0 to 3 and higher scores mean worse outcome. At the 4th, 12t, 20th and 24th week
Other Questionnaires_Constitution in Chinese Medicine Questionnaire (CCMQ);Scoring from 1 to 5 and higher scores correspond to specific body constitution. At the 4th, 12th, 20th and 24th week
Other 6 minutes walking test (6 minutes walking distance, meters) At the 4th, 12t, 20th and 24th week
Other Left ventricular ejection fraction (Ejection fraction, %) At the 24th week
Other Heart rate variability_SDNN (Standard deviation of all normal to normal intervals, ms) At the 12th and 24th week
Other Heart rate variability_SDANN index (Standard deviation of average normal to normal intervals index, ms) At the 12th and 24th week
Other Heart rate variability_ASDNN (Average standard deviation of all 5-min R-R intervals, ms) At the 12th and 24th week
Other Heart rate variability_rMSSD (The square root of the mean of the sum of the squares of differences between adjacent NN intervals, ms) At the 12th and 24th week
Other Heart rate variability_LF (Low frequency power, normalized unit/ n.u. and ms2) At the 12th and 24th week
Other Heart rate variability_HF (High frequency power, normalized unit/ n.u. and ms2) At the 12th and 24th week
Other Heart rate variability_LF/HF (LF/HF Ratio) At the 12th and 24th week
Primary N- terminal pro-brain natriuretic peptide, NT-proBNP The change of NT-pro BNP from the date of admission to the end of trial At the 12th week and 24th week
Secondary High sensitivity C-Reactive Protein, hs-CRP Hs-CRP The change of NT-pro BNP from the date of admission to the end of trial At the 12th week and 24th week
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