Skip to content

Protective effect of Sacubitril/Valsartan on residual renal function in peritoneal dialysis patients: a multicenter, prospective, open label, randomized controlled study

Protective effect of Sacubitril/Valsartan on residual renal function in peritoneal dialysis patients: a multicenter, prospective, open label, randomized controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054733
Enrollment
Unknown
Registered
2021-12-25
Start date
2021-12-20
Completion date
Unknown
Last updated
2022-12-05

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

Conditions

Peritoneal dialysis

Interventions

Treatment group:Sacubitril/Valsartan

Sponsors

the First Affiliated Hospital of Anhui University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years, male or female; 2. Maintaining peritoneal dialysis for more than 3 months; 3.24 Urine volume >= 400 ml/d; 4. Blood pressure >= 120/70mm Hg.

Exclusion criteria

Exclusion criteria: 1. Myocardial infarction, unstable angina pectoris, cardiovascular reconstruction surgery (such as stent or bypass surgery) or cerebrovascular accident within 6 months before screening, or planning to undergo cardiovascular reconstruction surgery during the trial; 2. Subjects who have previously received kidney transplantation and are currently receiving immunosuppressive therapy; 3. Patients who have used ACEI/ARB drugs or sacubitril-valsartan tablets within 1 month before screening; 4. Severe liver disease, such as acute hepatitis, chronic active hepatitis, cirrhosis, or alanine aminotransferase or aspartate aminotransferase levels exceeding 2.0 times the upper limit of normal; 5. Alcoholism or drug abuse, cachexia and mental disorders; 6. Patients who use diuretics for a long time; 7. Known allergy or intolerance to sacubitril and valsartan; 8. Have participated in or are participating in other clinical trials one month before screening.

Design outcomes

Primary

MeasureTime frame
Anuria;

Secondary

MeasureTime frame
Residual kidney GFR;Peritoneal and residual kidney kt / V;Peritoneal and residual renal Ccr;All cause death;Incidence of cardiovascular events;N-terminal natriuretic peptide precursor levels;Left ventricular ejection fraction;24-hour mean systolic blood pressure (mmHg) and mean diastolic blood pressure (mmHg);Hemoglobin level;Serum electrolyte level;

Countries

China

Contacts

Public ContactWang Yiping

the First Affiliated Hospital of Anhui University of Chinese Medicine

wypwyp54@aliyun.com+86 13075580986

Outcome results

None listed

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