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The Relationship Between XinKang-I and Chronic Heart Failure

Primary Purpose

Traditional Chinese Medicine

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Traditional Chinese medicine prescription:XinKang-I
Sponsored by
Dongguan Hospital of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traditional Chinese Medicine

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: History of CHF or clinical findings of CHF for more than 3 months. CHF was diagnosed in accordance with the European Society of Cardiology's 2021 Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure. Patients ranged in age from 18 to 85. Cardiac function was graded at grade II-IV (New York Heart Association functional class). Patients who had not used traditional Chinese medicine for treating heart failure within 1 week before enrollment; Written informed consent will be obtained. Exclusion Criteria: acute cardiac insufficiency, acute myocarditis, severe valvular heart disease, malignant arrhythmia, obstructive cardiomyopathy, pericardial tamponade, constrictive pericarditis or acute coronary syndrome severe lung, liver or kidney dysfunction nervous and hematopoietic system malignant tumors hemodynamic nstability pulmonary embolism severe infection pregnant or lactating refusal to provide written informed consent for this study

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    No Intervention

    Arm Label

    intervention group

    The control group

    Arm Description

    The intervention group will receive not only Western medicine, but also XK-I. The therapeutic drugs used in the control group will be according to the European Society of Cardiology's 2021 guidelines for the diagnosis and treatment of acute and chronic heart failure.

    The control group will receive Western medicine.The therapeutic drugs used in the control group will be according to the European Society of Cardiology's 2021 guidelines for the diagnosis and treatment of acute and chronic heart failure.

    Outcomes

    Primary Outcome Measures

    The changes in 6-minute walking distance(distance, meter).
    Cardiac function
    oxygen consumption volume of anaerobic threshold (VO2AT, ml)
    Cardiac function
    maximum oxygen volume uptake (VO2max, ml/min) in cardiopulmonary function test
    Cardiac function

    Secondary Outcome Measures

    Full Information

    First Posted
    April 13, 2023
    Last Updated
    May 5, 2023
    Sponsor
    Dongguan Hospital of Traditional Chinese Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05847959
    Brief Title
    The Relationship Between XinKang-I and Chronic Heart Failure
    Official Title
    The Relationship Between XinKang-I and Chronic Heart Failure: Protocol for a Randomized Controlled Study.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    May 1, 2023 (Anticipated)
    Primary Completion Date
    December 31, 2025 (Anticipated)
    Study Completion Date
    December 31, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Dongguan Hospital of Traditional Chinese Medicine

    4. Oversight

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

    5. Study Description

    Brief Summary
    Background: Heart failure is the severe and terminal stage of various heart diseases, which is characterized by high morbidity, mortality and readmission. There are few studies on the relationship between XinKang-I(XK-I) and chronic heart failure. Objective: To explore the relationship between XK-I and chronic heart failure. Methods/design: The trial is a single-center, single-blind, randomized study (1:1). It will recruit 110 patients with chronic heart failure who syndrome of qi deficiency yang deficiency and blood stasis. The intervention group will receive not only Western medicine, but also XK-I. The primary end points will be the changes in oxygen consumption volume of anaerobic threshold (VO2AT), maximum oxygen volume uptake (VO2max), and 6-minute walking distance after 8 weeks of treatment. Both groups will receive 8 weeks of treatment. Ethics and dissemination: Ethical approval was granted by Ethics Committee of Dongguan TCM Hospital. Results will be disseminated via peer-reviewed publications and presentations at international conferences.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Traditional Chinese Medicine

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    110 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    intervention group
    Arm Type
    Active Comparator
    Arm Description
    The intervention group will receive not only Western medicine, but also XK-I. The therapeutic drugs used in the control group will be according to the European Society of Cardiology's 2021 guidelines for the diagnosis and treatment of acute and chronic heart failure.
    Arm Title
    The control group
    Arm Type
    No Intervention
    Arm Description
    The control group will receive Western medicine.The therapeutic drugs used in the control group will be according to the European Society of Cardiology's 2021 guidelines for the diagnosis and treatment of acute and chronic heart failure.
    Intervention Type
    Drug
    Intervention Name(s)
    Traditional Chinese medicine prescription:XinKang-I
    Intervention Description
    XK-I will be used in intervention group (20 grams of radix astragalus, 20 grams of radix codonopsis, 10 grams of stir-fried semen lepidii, 8 grams of sweet apricot kernel, 10 grams of cassia twig, 15 grams of poria cocos, 10 grams of atractylodes, 5 grams of honey-roasted licorice, 15 grams of radix et rhizoma salviae miltiorrhizae, 10 grams of chuanxiong rhizoma, 5 grams of tangerine peel).Patients will take XK-I once a day, divided into morning and evening administration. The treatment lasted for 8 weeks.
    Primary Outcome Measure Information:
    Title
    The changes in 6-minute walking distance(distance, meter).
    Description
    Cardiac function
    Time Frame
    8 weeks
    Title
    oxygen consumption volume of anaerobic threshold (VO2AT, ml)
    Description
    Cardiac function
    Time Frame
    8 weeks
    Title
    maximum oxygen volume uptake (VO2max, ml/min) in cardiopulmonary function test
    Description
    Cardiac function
    Time Frame
    8 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    85 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: History of CHF or clinical findings of CHF for more than 3 months. CHF was diagnosed in accordance with the European Society of Cardiology's 2021 Guidelines for the Diagnosis and Treatment of Acute and Chronic Heart Failure. Patients ranged in age from 18 to 85. Cardiac function was graded at grade II-IV (New York Heart Association functional class). Patients who had not used traditional Chinese medicine for treating heart failure within 1 week before enrollment; Written informed consent will be obtained. Exclusion Criteria: acute cardiac insufficiency, acute myocarditis, severe valvular heart disease, malignant arrhythmia, obstructive cardiomyopathy, pericardial tamponade, constrictive pericarditis or acute coronary syndrome severe lung, liver or kidney dysfunction nervous and hematopoietic system malignant tumors hemodynamic nstability pulmonary embolism severe infection pregnant or lactating refusal to provide written informed consent for this study

    12. IPD Sharing Statement

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    The Relationship Between XinKang-I and Chronic Heart Failure

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