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Clinical Study on the Immunomodulatory Effect of Eprolidone on Patients with Chronic Heart Failure

Clinical Study on the Immunomodulatory Effect of Eprolidone on Patients with Chronic Heart Failure

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074711
Enrollment
Unknown
Registered
2023-08-14
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Chronic heart failure

Interventions

Conventional treatment group:Other conventional anti chronic heart failure drugs taking non Aldosterone receptor blockers for 4 consecutive weeks
Eprolidone group:Take regular medication and combine with 25 mg/day of Eprolidone, gradually increasing to 50 mg/day, for 4 consecutive weeks.

Sponsors

College of Pharmacy, Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Sign informed consent form, NYHA Level I, Level II ? The left ventricular Ejection fraction (LVEF) measured by radionuclide ventriculography (RNVG) is = 45% after the diagnosis of Grade I chronic congestive heart failure.

Exclusion criteria

Exclusion criteria: Age80, serum creatinine level>2.5 mg/dL, blood potassium level>5.0 mmol/L, surgical treatment of valvular heart disease, Contraindication to the study drug, use of other Aldosterone receptor antagonists, malignant tumors and other life-threatening non heart diseases, legally incapacitated patients, drug and alcohol abuse history, pregnant women and postpartum women, women who breast fed during the study period.

Design outcomes

Primary

MeasureTime frame
Treg cell activity in circulation;Formaldehyde solid level in the cycle;The level of inflammatory factors in plasma;Cardiovascular hospitalization;

Secondary

MeasureTime frame
clinical status;Patient quality related to patient health;

Countries

China

Contacts

Public ContactChengLu feng

College of Pharmacy, Xinjiang Medical University

Lewis_clf@163.com+86 139 9915 1882

Outcome results

None listed

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