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A multicenter prospective non-randomized control study of icodextrin peritoneal dialysis for the prevention and treatment of major adverse cardiovascular events in patients with peritoneal dialysis

A multicenter prospective non-randomized control study of icodextrin peritoneal dialysis for the prevention and treatment of major adverse cardiovascular events in patients with peritoneal dialysis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065980
Enrollment
Unknown
Registered
2022-11-21
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

end stage kidney disease

Interventions

group ICO:Icodextrin peritoneal dialysis fluid
control group GLU :glucose PD fluid

Sponsors

Shanghai East Hospital (East Hospital Affiliated to Tongji University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years (including 18 and 75 years old), gender, ethnicity, dialysis age is not limited; 2. CAPD and stable dialysis for more than 3 months; 3. Life expectancy greater than 1 year; 4. The patient signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Less than 3 months of peritoneal dialysis; 2. Received automated peritoneal dialysis and received icodextrin solution prior to enrollment; 3. Patients with advanced malignant tumors, liver cirrhosis and severe liver insufficiency, severe infection, active tuberculosis, acute myocardial infarction within three months before entering the study, history of major surgical trauma within three months, peritonitis within three months, etc.; 4. Have hepatitis B or HIV seropositive, or are receiving immunosuppressive medications; 5. From hemodialysis and kidney transplantation to abdominal dialysis; 6. Hypersensitivity to icodextrin dialysate; 7. The patient refused to participate in the study.

Design outcomes

Primary

MeasureTime frame
survival analysis;major advance cardiac event;

Secondary

MeasureTime frame
Bioimpedance body composition analysis;

Countries

China

Contacts

Public ContactLiu Na

Shanghai East Hospital (East Hospital Affiliated to Tongji University)

naliubrown@163.com+86 18918958730

Outcome results

None listed

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