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Application of high-flux hemodialysis combined with hypoxia -inducible factor prolyl hydroxylase inhibitor in the prevention and treatment of renal anemia in patients with uremia

Application of high-flux hemodialysis combined with hypoxia -inducible factor prolyl hydroxylase inhibitor in the prevention and treatment of renal anemia in patients with uremia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095158
Enrollment
Unknown
Registered
2025-01-02
Start date
2022-04-25
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

enal anemia

Interventions

Group one:LFHD+rhEPO
Group two:HFHD+rhEPO
Group three:HFHD+HIF-PHI

Sponsors

Rongchang District People's Hospital of Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis: Chronic renal failure, uremia (CKD stage 5). Diagnostic criteria: Creatinine clearance rate = 707 umol/L, with dialysis frequency of no less than 3 times per week (2020 KDIGO guidelines). 2.Meet the criteria for anti-anemia treatment in dialysis patients: Hemoglobin < 100g/L. 3.The medical record data is complete, and regular hemodialysis treatment has been carried out in our hospital for more than 3 months.

Exclusion criteria

Exclusion criteria: (1) Patients who received treatments for increasing HB within one month. (2) Patients who used hormones or cytotoxic drugs within the recent three months. (3) Patients who had a history of blood transfusion or intravenous use of iron supplements within three months. (4) Patients with chronic bleeding. (5) Severe malnutrition, liver insufficiency, heart failure, gastric ulcer or blood disorders. (6) Dialysis time is less than three months or the patient cannot adhere to regular hemodialysis. (7) The patient is not voluntarily participating in this study, or withdraws due to changes in condition, death or personal request during the study.

Design outcomes

Secondary

MeasureTime frame
Hematocrit;serum ferritin;total iron-binding capacity;Transferrin saturation;

Primary

MeasureTime frame
hemoglobin;

Countries

China

Contacts

Public ContactGuo Jiguang

Rongchang District People's Hospital of Chongqing

86736844@qq.com+86 158 0232 2267

Outcome results

None listed

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