- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06403176
Arteriovenous Plasma Multiomics in Patients With Disorders of Consciousness
Arteriovenous Plasma Multiomics and Inflammatory Factors in Patients With Disorders of Consciousness
Study Overview
Status
Intervention / Treatment
Detailed Description
Background:It is unclear what substances the brain needs to ingest for its activity under pathological conditions
Method:The uptake and release of substances by the brain were observed by comparing arterial blood with internal jugular vein blood;The characteristics of brain metabolites were observed by comparing internal jugular vein blood with superior vena cava blood. Compared it with the peripheral plasma metabolome of two additional patient cohorts: those in-stent restenosis and non-restenosis.
Objective:By analyzing different substances, this paper briefly describes the pathological mechanism of patients with disorders of consciousness, and looks for potential prognostic biomarkers.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Zhejiang
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Hanzhou, Zhejiang, China, 310003
- The First Affiliated Hospital of Zhejiang University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
1.Patients with consciousness disorder caused by various severe brain injuries
Exclusion Criteria:
- Patients who have been judged brain dead
- There are persistent epileptic activity, inhibition or seizure inhibition patterns
- Recent fever, abnormal liver and kidney function
- Previous history of neurological or mental illness
- Have a history of tumor
- Inflammatory bowel diseases, hyperlipidemia, gastritis
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Minimally conscious state (MCS)
Minimally conscious state (MCS): have reproducible signs of awareness and exhibit fluctuations in consciousness
|
No intervention
|
|
Vegetative state (VS)
Vegetative state (VS): can open their eyes and preserve sleep-wake cycles, but unaware of themselves and their surroundings
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No intervention
|
|
Patients with In-Stent Restenosis
In-Stent Restenosis was defined as greater than 50% within or immediately adjacent (within 5 mm) to the stent implanted that was detected by digital subtraction angiography (DSA).
|
No intervention
|
|
Patients with Non-Restenosis
In-Stent Restenosis was defined as less than 50% within or immediately adjacent (within 5 mm) to the stent implanted that was detected by digital subtraction angiography (DSA).
|
No intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient clinical outcome
Time Frame: 12 months
|
The patients were followed up for 12 months after blood collection to observe the clinical outcome
|
12 months
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Mental Disorders
- Cardiovascular Diseases
- Vascular Diseases
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Neurologic Manifestations
- Neurobehavioral Manifestations
- Neurocognitive Disorders
- Brain Ischemia
- Ischemic Attack, Transient
- Consciousness Disorders
Other Study ID Numbers
- plasma multiomics
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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