The Correlation and Mechanistic Study of GGCX Gene With Prognosis in Acute Ischemic Stroke
Study Protocol on the Correlation and Mechanistic Study of GGCX Gene With Prognosis in Acute Ischemic Stroke
2 other identifiers
observational
1,500
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2026
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 25, 2025
CompletedFirst Posted
Study publicly available on registry
December 8, 2025
CompletedStudy Start
First participant enrolled
January 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 28, 2028
December 8, 2025
November 1, 2025
7 months
November 25, 2025
November 25, 2025
Conditions
Keywords
Outcome Measures
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).
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.
Study Arms (1)
Acute Ischemic Stroke Group
These subjects were acute ischemic stroke patients who had been followed up for 3-12 months after discharge.
Interventions
The conventional drug therapy includes anticoagulant, antiplatelet, antihypertensive and other drugs. The surgical therapy includes AIS intravenous thrombolysis or endovascular therapy.
Eligibility Criteria
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.
You may qualify if:
- 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.
You may not qualify if:
- 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.
- Patients with severe cardiovascular, pulmonary, or hepatic diseases.
- Renal dysfunction.
- Cancer patients.
- Patients with active gastric ulcers or gastric bleeding.
- Pregnant or lactating patients.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University Aerospace Center Hospital
Beijing, China
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 12 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Researcher
Study Record Dates
First Submitted
November 25, 2025
First Posted
December 8, 2025
Study Start
January 25, 2026
Primary Completion (Estimated)
August 31, 2026
Study Completion (Estimated)
February 28, 2028
Last Updated
December 8, 2025
Record last verified: 2025-11