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Blood Proteome Profiling Identifies Biomarkers in Ischemic Stroke

The Blood Proteome Profiling Identifies Biomarkers Associated with Prognosis in Ischemic Stroke Due to Large Artery Atherosclerosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06729385
Enrollment
80
Registered
2024-12-11
Start date
2024-12-01
Completion date
2025-02-20
Last updated
2025-02-21

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

Conditions

Stroke

Brief summary

Endovascular thrombectomy and intravenous thrombolysis have become key therapeutic approaches for acute ischemic stroke. However, due to time window limitations, many patients are unable to receive reperfusion therapy, and the majority only receive supportive treatment. Ischemic stroke-related complications, including edema and infection, gradually subside after 7 days post-stroke, with the patient's condition generally stabilizing. Endogenous repair mechanisms will play a critical role in the coming months. This study aims to predict prognostic biomarkers for ischemic stroke patients who have not undergone reperfusion therapy, using blood proteomics data. All samples in our study are derived from this experiment. Our goal is to elucidate the molecular mechanisms underlying post-reperfusion prognosis and to provide insights for optimizing stroke treatment strategies.

Interventions

DIAGNOSTIC_TESTThe blood Proteome Profiling

Patients who meet the inclusion criteria will undergo fasting blood collection for proteomics analysis upon admission.

Sponsors

Capital Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18. * Clinical signs consistent with acute ischemic stroke (TOAST classification: large artery atherosclerosis) * 7 to 30 days from symptom onset.

Exclusion criteria

* Severe infection or multiple organ failure. * Untreated moderate or severe coronary artery stenosis, or a history of coronary artery bypass surgery. * Ongoing hemodialysis or peritoneal dialysis, or severe renal insufficiency characterized by a glomerular filtration rate (GFR) of less than 30 ml/min or serum creatinine levels exceeding 220 mmol/L (2.5 mg/dl). * Known intracranial aneurysm or cerebral arteriovenous malformation. * Malignant brain tumor or central nervous system (CNS) infection. * Pre-existing neurological or psychiatric conditions that could confound the neurological or functional assessments. * Baseline platelet count \<50 × 109/L. * Pregnancy or lactation at the time of admission.

Design outcomes

Primary

MeasureTime frameDescription
Primary Outcome Measures:3 monthsModified Rankin Scale score (mRS) at 90 days The Modified Rankin Scale (mRS) at 90 days was used to assess functional outcomes. The mRS is a widely utilized scale to measure the degree of disability or dependence in daily activities among stroke patients. Minimum value: 0 (indicating no symptoms or disability) Maximum value: 6 (indicating death) Interpretation: Higher scores represent worse outcomes, reflecting greater levels of disability or mortality.

Countries

China

Outcome results

None listed

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