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A Study on the Clinical Efficacy of Modified Guizhi Gancao Longgu Muli Decoction in Heart Failure with Preserved Ejection Fraction

A Study on the Clinical Efficacy of Modified Guizhi Gancao Longgu Muli Decoction in Heart Failure with Preserved Ejection Fraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002021
Enrollment
Unknown
Registered
2025-10-28
Start date
2023-01-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

heart failure with preserved ejection fraction

Interventions

treatment group:standard therapy plus modified Guizhi Gancao Longgu Muli decoction

Sponsors

Nanjing Municipal Health Commission
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 94 Years

Inclusion criteria

Inclusion criteria: The cases were selected from patients with heart failure admitted to the Department of Cardiology of Jiangning Hospital of Traditional Chinese Medicine in Nanjing City. The inclusion criteria were as follows: (1) Admission date from January 1, 2023 to December 31, 2024; (2) LVEF = 50%; (3) Elevated BNP, along with at least one of the following evidence of cardiac structural abnormalities (left ventricular hypertrophy, left atrial enlargement, abnormal diastolic function); (4) Exclusion of other non-cardiac factors causing dyspnea, edema, etc.; (5) NYHA classification of grade II to III; (6) During the observation period, patients could adhere to outpatient follow-up, take medication on time, and had good medication compliance. (7) All enrolled patients signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with heart failure not diagnosed as having "deficiency of heart yang" in traditional Chinese medicine. (2) Patients with HFrEF with LVEF 2 times the upper limit of normal. (6) Patients with moderate to severe renal function impairment (GFR = 60 ml/min or Cr = 186 µmol/L). (7) Patients with hyperkalemia before treatment (serum potassium > 5.3 mmol/L). (8) Patients with a history of angioedema related to ACEI or ARB drugs, or those with hereditary or idiopathic angioedema. (9) Pregnant or lactating women. (10) Patients with malignant tumors or other severe chronic wasting diseases.

Design outcomes

Primary

MeasureTime frame
Minnesota Living with Heart Failure Questionnaire;6-minute walk test;

Secondary

MeasureTime frame
mitral early diastolic velocity;mitral atrial velocity;E/e' ratio;B-type natriuretic peptide;type III procollagen amino terminal peptide;Major adverse cardiovascular events;

Countries

China

Contacts

Public ContactJiayang Xu

Nanjing Jiangning Hospital of Traditional Chinese Medicine

jiayangxu_29184@163.com+8613611504926

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026