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Clinical study on the treatment of frailty of patients with chronic heart failure and glucose and lipid metabolism disorder by Chinese herbal medicine for warming Spleen and reducing turbidity

Clinical study on the treatment of frailty of patients with chronic heart failure and glucose and lipid metabolism disorder by Chinese herbal medicine for warming Spleen and reducing turbidity

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080387
Enrollment
Unknown
Registered
2024-01-29
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

Frailty

Interventions

Treatment group:Standard Western medicine and Warming Spleen and Reducing Turbidity Decoction
Control group:Standard Western medicine

Sponsors

Guang’anmen Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age 30-80 years of age, gender not limited; (2) The glucolipid metabolic disorder and CHF diagnosis standard, cardiac function class (NYHA) ? - ?; (3) Comply with the Fried weak phenotypic 3 and above; (4) The diagnostic criteria of spleen deficiency and phlegm turbid syndrome; (5) Voluntary participants subjects and signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Caused by primary diseases (chronic kidney disease, chronic liver disease, hypothyroidism) of blood sugar, blood lipid abnormalities. (2) A diagnosis of type 1 diabetes, gestational diabetes, or other special types of diabetes. (3) The result of valvular heart disease, congenital heart disease, myocarditis caused by heart failure; (4) In acute coronary syndrome, severe arrhythmia and always happens every source sex shock; (5) And severe liver function abnormal ALT and AST (more than three times the upper limit of normal) or abnormal renal function (estimated glomerular filtration rate < 30 ml/min / 1.73 m2); (6) Patients with malignant tumors or autoimmune diseases; (7) Visual impairment, hearing disabled or cognitive impairment, and patients who are unable to cooperate with the scale test; (8) Allergic constitution and allergy to the components of the drug used in this study; (9) Be in other clinical trials or involved in other drugs clinical experiment is over not more than 1 months; (10) Women in pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Short Physical Performance Battery;

Secondary

MeasureTime frame
Kansas City Cardiomyopathy Questionnaire; Montreal Cognitive Assessment ;Geriatric Depression scale;Fasting blood glucose;2 hours postprandial blood sugar;HbA1c;total cholesterol;triglyceride;high-density lipoprotein;low-density lipoprotein;NT-proBNP;cTNI;Cardiac ultrasound;tumor necrosis factor-a;interleukin-6;interleukin-10;hsCRP;Monocytechemoattractantprotein-1;Intestinal flora;

Countries

China

Contacts

Public ContactLi Yumeng

Guang’anmen Hospital, China Academy of Chinese Medical Sciences

lym0707@163.com+86 156 5260 9020

Outcome results

None listed

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