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Clinical Trials in China / NCT07269288
Starting soon Observational

The Correlation and Mechanistic Study of GGCX Gene With Prognosis in Acute Ischemic Stroke

NCT07269288 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Aerospace Center Hospital
Phase
Observational
Started
2026-01-25
Last updated
2025-12-08

Condition(s) studied

Acute Ischemic Stroke

Investigational drug(s) / intervention(s)

Usually, all enrolled patients with acute ischemic stroke will receive routine medication and/or surgical treatment according to clinical diagnosis and treatment protocols.

Usually, all enrolled patients with acute ischemic stroke will receive routine medication and/or surgical treatment according to clinical diagnosis and treatment protocols.: The conventional drug therapy includes anticoagulant, antiplatelet, antihypertensive and other drugs. The surgical therapy includes AIS intravenous thrombolysis or endovascular therapy.

Study summary

This observational study aims to investigate the impact of GGCX gene mutations and GGCX levels on stroke prognosis in patients with ischemic stroke, as well as their correlation. The main issues are:

What is the relationship and potential mechanism between GGCX gene mutations and their expression levels and the composite prognosis of recurrence, death, and bleeding events in patients with ischemic stroke? Collect blood samples from enrolled ischemic stroke patients for genetic testing, and conduct follow-up visits at 3, 6, and 12 months after discharge to evaluate clinical prognosis outcomes. This will answer questions about the relationship and mechanism between GGCX gene and patient prognosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
Accepted
* Inclusion Criteria (1) Inclusion Criteria for Acute Ischemic Stroke Patients: 1. Aged between 18 and 85 years. 2. Diagnosed with ischemic stroke (in accordance with the "Chinese Guidelines for Diagnosis and Treatment of Acute Ischemic Stroke 2023," including TOAST etiological/pathogenic subtypes: large-artery atherosclerosis (LAA), cardioembolism (CE), small-artery occlusion (SAO), stroke of other determined etiology (SOE), and stroke of undetermined etiology (SUE)). 3. Acute onset, with symptoms occurring within 72 hours and being the first episode. 4. Voluntary participation with signed informed consent. (2) Inclusion Criteria for Healthy Controls: 1) Healthy control population matched for age, gender, and risk factors (including personal and family history). * Exclusion Criteria (1) Exclusion Criteria for Healthy Controls: 1. Patients with cerebrovascular diseases occurring within 72 hours. 2. Pregnant or lactating patients. (2) Exclusion Criteria for Acute Ischemic Stroke Patients: 1. Other types of stroke, including hemorrhagic stroke, mixed stroke, and tumor-related stroke patients. 2. Patients with coagulation disorders or other hematologic diseases. 3. Patients with severe cardiovascular, pulmonary, or hepatic diseases. 4. Renal dysfunction. 5. Cancer patients. 6. Patients with active gastric ulcers or gastric bleeding. 7. Pregnant or lactating patients.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking University Aerospace Center Hospital Beijing China

More Peking University Aerospace Center Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07269288 on ClinicalTrials.gov ↗ ← All trials in China