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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05555836
Other study ID # CFH2022-2-2081
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date December 31, 2024

Study information

Verified date September 2022
Source Beijing Shijitan Hospital, Capital Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The prevalence of cognitive impairment in maintenance hemodialysis (MHD) patients is 3 to 5 times higher than that in ordinary people, so it is essential to find the associated risk factors in this population. This project intends to evaluate whether changes in cerebral blood flow during dialysis have an impact on cognitive function in middle-aged and elderly MHD patients and clarify their influence on brain imaging characteristics. MHD patients who started hemodialysis at 3 to 6 months were selected to examine the difference in middle cerebral artery flow rate before and after dialysis by transcranial Doppler ultrasound to reflect the changes in cerebral blood flow. Changes in the cognitive function scale assessment (memory, executive function, and other five cognitive domains) and brain magnetic resonance imaging examinations are planned to collect both at baseline and after a one-year follow-up. Then the investigator used the multiple linear regression method to analyze the effects of the difference in middle cerebral artery flow on the changes in cognitive function and the characteristics in brain imaging. The investigators anticipate that the characteristics of the influence of changes in cerebral blood flow on cognitive impairment in Chinese MHD patients will be elucidated in this study, which may provide crucial clinical evidence for finding preventive and intervention measures for cognitive impairment in this group of population.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 121
Est. completion date December 31, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - Age greater than 50, no gender limitation; - End-stage renal disease, stable dialysis for 3-6 months; - Subjects voluntarily participated in the study and signed informed consent, and were able to participate in clinical data collection, neuropsychological assessment, transcranial Doppler ultrasound (TCD), head MRI, and 1-year follow-up. Exclusion Criteria: - Congenital mental retardation or disturbance of consciousness, schizophrenia, or history of severe anxiety and depression (Hamilton Depression Scale score more than 17; - Long-term alcohol or psychotropic drug dependence; - Those who cannot complete the neuropsychological assessment due to visual impairment, hearing impairment, or limb dysfunction; less than 10 hours of dialysis per week; - Patients with poor detection of the bilateral temporal window by TCD examination and unable to cooperate with ultrasound examination; - Those who cannot undergo head MRI examination for various reasons.

Study Design


Locations

Country Name City State
China Beijing Shijitan Hospital affiliated to Capital Medical University Beijing

Sponsors (1)

Lead Sponsor Collaborator
Beijing Shijitan Hospital, Capital Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in cognitive function which is measured by MoCA scores changes after 1 year follow-up This study is going to apply neuropsychological battery tests in MoCA assessment and evaluate the changes of MoCA scores of MHD patients after one year of follow-up. This measurement is going to be completed within 1 year after the last participant enrolls
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