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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorPeking University Aerospace Center Hospital

About this trial

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 criteria

This trial accepts healthy volunteers

Qualifiers

Aged between 18 and 85 years.

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)).

Acute onset, with symptoms occurring within 72 hours and being the first episode.

Voluntary participation with signed informed consent.

Disqualifiers

Patients with cerebrovascular diseases occurring within 72 hours.

Pregnant or lactating patients.

Other types of stroke, including hemorrhagic stroke, mixed stroke, and tumor-related stroke patients.

Patients with coagulation disorders or other hematologic diseases.

Trial population

This study will be conducted in six hospitals (centers) across the country, namely Xi'an Jiaotong University First Affiliated Hospital, Shandong Weifang Second People's Hospital, Shandong Linshu People's Hospital, Hunan Second People's Hospital (Hunan Brain Hospital), and Nantong First People's Hospital.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

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

    Combination product

    The conventional drug therapy includes anticoagulant, antiplatelet, antihypertensive and other drugs. The surgical therapy includes AIS intravenous thrombolysis or endovascular therapy.

Treatment groups

1,500 Participants
are divided into 1 treatment group
Group A: Acute Ischemic Stroke Group1 intervention

Trial outcomes

Primary outcomes

1

Evaluate the recurrence, death, and bleeding events of stroke in the research subjects

Including recurrent ischemic stroke events; Death events include hemorrhagic death, vascular death, and acute myocardial infarction events; Intracranial or other bleeding events (refer to the International Classification of Bleeding Events ICD-10 code).

Time frame
Follow up will be conducted at 3 months, 6 months, and 12 months after the patient's discharge, and the main outcome events mentioned above will be evaluated.

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Peking University Aerospace Center Hospital

Lead sponsor

Aerospace Center Hospital

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: