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Application of sacubarb / valsartan in maintenance hemodialysis patients with preserved ejection fraction heart failure: a single arm study

Application of sacubarb / valsartan in maintenance hemodialysis patients with preserved ejection fraction heart failure: a single arm study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100042186
Enrollment
Unknown
Registered
2021-01-15
Start date
2021-01-18
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

End Stage Renal Disease, Heart Failure

Interventions

experimental group:sacubarb/valsartan taken

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Male or female patients aged 18-80 years; 2. Qualitative diagnosis: chronic renal failure patients, glomerular filtration rate 40%, but abnormal ventricular diastolic function (according to PARAGON-HF study, E / E 'value, septal and lateral wall e' velocity, left atrial maximum volume index (LAMVI), and maximum tricuspid regurgitation velocity were analyzed). Echocardiography was performed by two doctors with more than 5 years of ultrasound experience in the Department of Cardiology, Peking Union Medical College Hospital. The ultrasound data were saved for follow-up analysis. 5. Patients or their family members can understand the study protocol and are willing to participate in the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant tumor or expected survival period is less than 6 months; 2. Severe liver disease; 3. Surgery is needed in the near future; 4. Pregnant or lactating women; women of childbearing age with positive or no pregnancy test at baseline. Postmenopausal women must be postmenopausal for at least 12 months; 5. Echocardiography showed new ventricular wall motion abnormalities, or symptoms of unstable angina pectoris, and ECG has the corresponding prompt. Or patients with myocardial infarction or unstable angina pectoris within 1 month according to clinical judgment; 6. Allergic to or contraindication to the drug components of sakubatro or valsartan; 7. Serum potassium > 5.4mmol/l; 8. Blood vessel edema happened after ACEI or ARB drugs used in the past; 9. The patients or their families can not understand and accept the conditions and objectives of this study.

Design outcomes

Primary

MeasureTime frame
E/e' value;E'velocity of interventricular septum and lateral wall;LAMVI;Maximum tricuspid regurgitation velocity;

Countries

China

Contacts

Public ContactXuemei Li, Zhicheng Jing

Peking Union Medical College Hospital, Chinese Academy of Medical Sciences

lixmpumch@126.com13911467356

Outcome results

None listed

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