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Association of Plasma Metabolomic Biomarkers with Chronic Ischemic White Matter Injury

Association of Plasma Metabolomic Biomarkers with Chronic Ischemic White Matter Injury

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06608251
Acronym
WML
Enrollment
100
Registered
2024-09-23
Start date
2024-06-01
Completion date
2025-05-31
Last updated
2024-09-23

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

Conditions

Myelinopathy

Brief summary

The cases were screened according to the inclusion criteria, and after the patients signed the informed consent, the clinical data were collected, the imaging data were evaluated, and blood samples were taken for follow-up measurements. In the early morning of the second day after the patient was enrolled, 5mL of peripheral venous blood was drawn and sent to the neurology laboratory of our hospital for separation, and the detection of plasma metabolomics markers was performed.

Detailed description

In the early morning of the second day after the patient was enrolled, 5mL of peripheral venous blood was drawn and sent to the neurology laboratory of our hospital for separation, and the detection of plasma metabolomics markers was performed.Inluding CRP,Complete blood count,Liver and kidney function indicators,et.

Interventions

DIAGNOSTIC_TESTwhite matter lesion

According to the results of magnetic resonance, they were divided into white matter degeneration group and non-white matter degeneration group

Sponsors

Nanjing First Hospital, Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

: 1. Be older than 45 years old; 2. Patients admitted to the Department of Neurology due to headache, vertigo, anxiety, etc.; 3. There were no symptoms of neurological deficit on physical examination; 4. Able to cooperate with the improvement of brain MRI examination; 5. Sign the informed consent form.

Exclusion criteria

1. History of stroke, traumatic brain injury, intracranial tumor, central nervous system infection, active malignant tumor, thyroid disease, autoimmune disease, active or chronic inflammatory disease, severe liver and kidney impairment, etc.; 2. accompanied by neurological deficit symptoms; 3. refusal to participate in the study; 4. Other conditions judged by the investigator to be unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frameDescription
myelinopathy2024.06.01-2027.06.01The degree of damage to the white matter of the brain is judged based on the magnetic resonance Fazekas score(1-3), with the higher scores indicating the damage more severe.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026