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Clinical cohort study of the effect of hypoxia-inducible factor prolyl hydroxylase inhibitor (roxadustat) on cognitive function in maintenance hemodialysis patients

Clinical cohort study of the effect of hypoxia-inducible factor prolyl hydroxylase inhibitor (roxadustat) on cognitive function in maintenance hemodialysis patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070478
Enrollment
Unknown
Registered
2023-04-13
Start date
2023-04-13
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Chronic kidney disease

Interventions

Erythropoietin group:NA

Sponsors

Deyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, dialysis 3 times a week, 3-4 hours each time, dialysis time >=3 months (Kt/V > 1.2, URR > 65%); 2. In patients diagnosed with renal anemia who were treated with rosalrestat or erythropoietin, Hb was controlled at 100-130g/L after treatment; 3. Clear consciousness, no mental dysfunction, can accurately express their own will; 4. All patients signed informed consent with complete clinical data.

Exclusion criteria

Exclusion criteria: 1. Anemia caused by diseases other than CKD, such as pure red cell aplastic anemia and myelodysplastic syndrome; 2. Patients with malignant tumors that affect their survival; 3. Poor compliance; 4. Any other circumstances in which the investigator considers the subject unable to participate in the study; 5. Patients with previous cerebrovascular disease or myocardial infarction; 6. Dementia patients; 7. Use of benzodiazepines; 8. A history of mental illness, such as depression or schizophrenia; 9. Patients have sensory (visual and auditory) or motor impairments that prevent them from completing tests that require these senses; 10. The patient has a life expectancy of less than 6 months, is scheduled for a kidney transplant within the baseline 6 months, or is expected to have a recovery of kidney function; 11. Severely impaired liver function; 12. Patients during lactation and pregnancy.

Design outcomes

Primary

MeasureTime frame
ß amyloid;Phosphorylated TaU-181 protein;Hypoxic inducible factor-1 a;Disintegrin-like metalloproteinase 10;Montreal Cognitive Assessment Scale;

Countries

China

Contacts

Public ContactLiu Minglin

Deyang People's Hospital

wj294141319@126.com+86 18280034120

Outcome results

None listed

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