NCT07269288

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

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,500

participants targeted

Target at P75+ for all trials

Timeline
22mo left

Started Jan 2026

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress14%
Jan 2026Feb 2028

First Submitted

Initial submission to the registry

November 25, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 8, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

January 25, 2026

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 31, 2026

Expected
1.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2028

Last Updated

December 8, 2025

Status Verified

November 1, 2025

Enrollment Period

7 months

First QC Date

November 25, 2025

Last Update Submit

November 25, 2025

Conditions

Keywords

Stroke

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.

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

Interventions

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

Acute Ischemic Stroke Group

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study 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.

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

Location

MeSH Terms

Conditions

Ischemic StrokeStroke

Interventions

Clinical Protocols

Condition Hierarchy (Ancestors)

Cerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

TherapeuticsEpidemiologic Study CharacteristicsHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and Evaluation

Central Study Contacts

Xia Zhang, PhD

CONTACT

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

Locations