Skip to content

Pathological Mechanisms of Sphingolipid Metabolism and Pyroptosis in Acute Ischemic Stroke: An Observational Study

Pathological Mechanisms of Sphingolipid Metabolism and Pyroptosis in Acute Ischemic Stroke: An Observational Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099885
Enrollment
Unknown
Registered
2025-03-31
Start date
2025-04-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Acute ischemic stroke

Interventions

Study Group:None
Control Group:None

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Study Group Inclusion Criteria: 1. Meet the diagnostic criteria for acute cerebral infarction; 2. Onset time=13 points; 5. Be between the ages of 18-85; 6. Meet the indications for intravenous thrombolysis of alteplase within 4.5 hours, and receive intravenous thrombolysis therapy with alteplase; 7. Volunteer to take the test and sign the informed consent form. Inclusion Criteria for the Control Group: 1. Meet the diagnostic criteria for high-risk groups of stroke; 2. Match the gender, age and underlying cardiovascular and cerebrovascular diseases of the subjects in the study group; 3. Volunteer to be tested and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Severe circulatory, respiratory, urinary, digestive, immune, hematologic diseases, or cancer, or acid sphingomyelinase deficiency; 2. Subjects with a history of schizophrenia, intellectual retardation, or other diseases that limit participation in the validity of informed consent or investigation in this study; 3. Recent use of antibiotics, non-steroidal anti-inflammatory drugs, hormones, immunosuppressants and other anti-inflammatory drugs, or taking amitriptyline, trimipramine, desipramine, fluoxetine and other acid sphingomyelinase inhibitors; 4. Patients with language impairment who cannot cooperate with the investigation; 5. Inability to comply with the study protocol.

Design outcomes

Primary

MeasureTime frame
Ceramide;Nucleotide-binding domain, leucine-rich repeat containing protein 3, NLRP3;Gasdermin D, GSDMD;

Secondary

MeasureTime frame
Interleukin-18, IL-18;Interleukin-1 beta, IL-1ß;

Countries

China

Contacts

Public ContactYunling Zhang

Xiyuan Hospital, China Academy of Chinese Medical Sciences

yunlingzhang2004@126.com+86 139 1076 4257

Outcome results

None listed

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