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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05847959
Other study ID # DongguanHTCM
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date December 31, 2025

Study information

Verified date April 2023
Source Dongguan Hospital of Traditional Chinese Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 110
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: 1. 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. 2. Patients ranged in age from 18 to 85. 3. Cardiac function was graded at grade II-IV (New York Heart Association functional class). 4. Patients who had not used traditional Chinese medicine for treating heart failure within 1 week before enrollment; 5. Written informed consent will be obtained. Exclusion Criteria: 1. acute cardiac insufficiency, acute myocarditis, severe valvular heart disease, malignant arrhythmia, obstructive cardiomyopathy, pericardial tamponade, constrictive pericarditis or acute coronary syndrome 2. severe lung, liver or kidney dysfunction 3. nervous and hematopoietic system 4. malignant tumors 5. hemodynamic nstability 6. pulmonary embolism 7. severe infection 8. pregnant or lactating 9. refusal to provide written informed consent for this study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Traditional Chinese medicine prescription:XinKang-I
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.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Dongguan Hospital of Traditional Chinese Medicine

Outcome

Type Measure Description Time frame Safety issue
Primary The changes in 6-minute walking distance(distance, meter). Cardiac function 8 weeks
Primary oxygen consumption volume of anaerobic threshold (VO2AT, ml) Cardiac function 8 weeks
Primary maximum oxygen volume uptake (VO2max, ml/min) in cardiopulmonary function test Cardiac function 8 weeks
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