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Status unknownNCT03961724NESRDUpdated Apr 28, 2022

Neuroimaging and End Stage Renal Disease

An observational study in End Stage Renal Disease, sponsored by First Affiliated Hospital Xi'an Jiaotong University. Status unknown at 1 site in China. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-28.

Sponsored by First Affiliated Hospital Xi'an Jiaotong University · Observational

The sponsor has not verified this record recently (last verified Apr 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
192
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Brain impairment is one of the common complications of end-stage renal disease (ESRD). The patients always present with various cerebrovascular diseases, cognitive impairment and sensorimotor abnormalities, with morbidity over 40%. However, the risk factors and the neural mechanisms of brain injury in ESRD is still unclear. Identifying the risk factors and finding objective and reliable biomarkers of brain impairment in the process of ESRD is an important clinical problem. At the same time, to find the neural mechanisms of brain damage in ESRD is a serious scientific problem. Neuroimaging techniques based on multi-modal magnetic resonance image (MRI) can detect the structural and functional brain abnormalities objectively and sensitively, especially for those without obvious clinical symptoms. Through the deep analysis of brain MRI data, it is helpful for studying the neural mechanisms of brain damage in ESRD in the perspective from brain science. In addition, the accumulation of uremic toxins is supposed to play an essential role in the brain impairment of ESRD. The metabolomics is a useful method in detecting the uremic toxins with different molecular weights. In this study, the investigators will collect the brain MRI, serum metabolomics and cognitive assessment data before the dialysis initiation, and then will make prospective longitudinal observation of changes of brain impairment during the dialysis. Thus, combining analysis of neuroimaging and metabolomics will provide more information for finding the risk factors and imaging diagnostic markers of brain impairment in ESRD. It will also helpful for explaining the underlying mechanisms of brain impairment in ESRD, providing an objective basis for clinical diagnosis and prediction of the prognosis.

02

Conditions studied

  • End Stage Renal Disease
03

In context

Kidney Diseases

3,838 studies on the registry are indexed under Kidney Diseases; 498 are open to participants now.

This study's planned enrollment of 192 is close to the median of 192 across 1,032 observational studies indexed under Kidney Diseases.

Browse Kidney Diseases studies →

Lead sponsor

First Affiliated Hospital Xi'an Jiaotong University is the lead sponsor of 306 studies on the registry; 86 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All of the patients of ESRD group are in-patients and out-patients in the nephrology department from three research centers. The subjects of control group are recruited from community.

Inclusion criteria

  • Diagnosis with end stage renal disease before dialysis initiation
  • Chronic renal failure
  • Chronic renal failure
  • 18-55 years old
  • Right handedness

Exclusion criteria

Exclusion Criteria:

  • Concurrent severe infection
  • With other severe diseases
  • History of central nervous system diseases, such as mental disorder, degenerative diseases of central nervous system, tumors, trauma, etc.
  • History of alcohol dependence and drug abuse
  • History of brain operation
  • Loss of vision or hearing
  • Psychotropic medication in three months
  • Contraindication of MRI examination, such as metal implants and claustrophobia, and other reasons that cannot cooperate with MRI examination
  • Cerebrovascular diseases which can be detected from conventional MR images, including the size of cerebral hemorrhage over 10 mm, infarction over 20 mm, subarachnoid hemorrhage, subdural hemorrhage and extradural hemorrhage.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
192 participants (estimated)
Patient registry
No

Groups and cohorts

  • ESRD group

    Device: magnetic resonance image (MRI)

  • Control group

    Device: magnetic resonance image (MRI)

Interventions

  • Devicemagnetic resonance image (MRI)

    serum metabolomics

    Also known as: serum

06

What researchers measure

Primary outcomes

  1. Change from baseline brain structure measures at 3 months and 12months

    The changes of brain volume (mm3) are evaluated by structural MRI

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

  2. Change from baseline brain function measures at 3 months and 12months

    The changes of brain functional connectivity intensity are evaluated by functional MRI

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

Secondary outcomes

  1. Changes from baseline cognitive condition at 3 months and 12months

    The cognitive condition is assessed by Montreal cognitive assessment (MoCA). The MoCA assesses several cognitive domains: 1) visuospatial and executive abilities are assessed using a trail-making test B (1 point), clock-drawing task (3 points) and a cube copy (1 point); 2) naming is assessed with low-familiarity animals (3 points); 3) the short-term memory (5 points) involves two learning trials of five nouns; 4) attention are evaluated using a sustained attention task (1 point), a serial subtraction task (3 points), and digits forward and backward (1 point each); 5) language is assessed using a repetition of two syntactically complex sentences (2 points), and the verbal fluency task (1 point); 6) orientation to time and place is evaluated by asking the subject for the date and the city (6 points). The scale ranges is from 0 to 30, and score of 26 or over is considered to be normal. Subscales are summed to compute a total score, and higher values represent a better outcome.

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

  2. Changes from baseline depression condition at 3 months and 12months

    The affective complaints are assessed by Beck depression inventory (BDI). The BDI is a 21-question multiple-choice self-report inventory in the past week, for measuring the severity of depression. The BDI is composed of items relating to symptoms of depression such as hopelessness and irritability, cognitions such as guilt or feelings of being punished, as well as physical symptoms such as fatigue, weight loss, and lack of interest in sex. Each question had a set of at least four possible responses, ranging in intensity: (0) I do not feel sad; (1) I feel sad; (2) I am sad all the time and I can't snap out of it; (3) I am so sad or unhappy that I can't stand it. When the test is scored, a value of 0 to 3 is assigned for each answer and then the total score is summed to be compared to a key to determine the depression's severity. The scale ranges is from 0 to 63, and the higher total scores indicate more severe depressive symptoms.

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

  3. Changes from baseline anxiety condition at 3 months and 12months

    The affective complaints are assessed by Beck anxiety inventory (BAI). The BAI is a 21-question multiple-choice self-report inventory that is used for measuring the severity of anxiety in children and adults. The questions used in this measure ask about common symptoms of anxiety that the subject has had during the past week (including the day you take it) (such as numbness and tingling, sweating not due to heat, and fear of the worst happening). The BAI contains 21 questions, each answer being scored on a scale value of 1 (not at all) ,2 (mild), 3 (moderate), to 4 (severely). The scale ranges is from 21 to 84 , and higher total scores indicate more severe anxiety symptoms.

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

  4. Changes from baseline serum metabolomics at 3 months and 12months

    The serum metabolomics are conducted by liquid Chromatograph Mass Spectrometer (LC-MS), mainly including the molecules of uremic toxins.

    Time frame: baseline (before dialysis initiation), hemodialysis for 3 months and 12 months

07

Study locations

1 of 1 sites recruiting
  • First Affiliated Hospital of Xian Jiaotong University
    Xian, Shaanxi 710061, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03961724
Lead sponsor
First Affiliated Hospital Xi'an Jiaotong University
Collaborators
215 Hospital of Shaanxi NI, Baoji Zhongxin Hospital, Taihe Hospital
Responsible party
Sponsor
First posted
May 23, 2019
Start date
Jul 1, 2019
Primary completion
Dec 31, 2022 (estimated)
Completion
Dec 31, 2022 (estimated)
Last update
Apr 28, 2022

Study contacts

Ming Zhang, PhD
Contact
zmmri@163.com
0086-18991232265
Shaohui Ma, MD
Contact
sh_ma@163.com
0086-15029215781
Ming Zhang, PhD
principal investigator · First Affiliated Hospital of Xian Jiaotong University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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