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Comparative study on the early prognosis of initial dialysis patients between the new sequential induction therapy of blood purification and the traditional induction dialysis

Comparative study on the early prognosis of initial dialysis patients between the new sequential induction therapy of blood purification and the traditional induction dialysis

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054573
Enrollment
Unknown
Registered
2021-12-20
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-11-28

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

Conditions

End-stages renal disease

Interventions

Control group:Traditional hemodialysis induced dialysis therapy
Experimental group:New sequential induction therapy of CRRT, hemodiafiltration and hemodialysis

Sponsors

The Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. At least 18 years old, regardless of gender; 2. Patients diagnosed with chronic renal failure and indicated for blood purification treatment, including uremic pericarditis, uremic encephalopathy, severe hyperkalemia, severe metabolic acidosis, pulmonary edema caused by water overload and other uremic complications; Patients with poor nutritional status, excessive water load, fatigue, cognitive impairment, metabolic acidosis, hyperkalemia and hyperphosphatemia that failed conservative treatment due to renal failure; 3. No previous history of blood purification treatment.

Exclusion criteria

Exclusion criteria: 1. Enter hemodialysis due to acute renal insufficiency and have no previous history of kidney disease; 2. Short-term conversion to peritoneal dialysis; 3. Kidney transplantation is planned during the trial period; 4. Mental disorders can not cooperate with treatment; 5. Pregnant and lactating women; 6. Have a previous or current malignant tumor (except excised non-melanoma skin cancer and carcinoma in situ); 7. History of severe allergies, such as allergic asthma, anaphylactic shock, severe gastrointestinal symptoms, etc.

Design outcomes

Primary

MeasureTime frame
Death;Rehospitalization rate;

Secondary

MeasureTime frame
Blood pressure;

Countries

China

Contacts

Public ContactXu Chengyun

The Second Affiliated Hospital of Nanchang University

1147202241@qq.com+86 13507916589

Outcome results

None listed

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