A Multicenter Study Based on Multi-omics Analysis to Predict the Early Prognosis and Recurrence Risk of Acute Ischemic Stroke

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Through a multicenter prospective AIS cohort study, we analyze the potential association of human proteome, microbiome and metabolome alterations with AIS prognosis, searching for key proteins, differential organisms and metabolites, combining experimental data at multiple molecular levels with computational models, and establishing early prediction models through machine learning-based prediction algorithms. While closely tracking the recurrence of stroke in AIS patients, we evaluate the predictive value of human proteome, microbiome and metabolites for stroke recurrence through a nested case-control study, which provides key reference information for exploring the unknown residual risk of AIS recurrence.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
View:

• Meet the diagnostic criteria of AIS according to the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018

• Aged 18 to 75 years old

• Stroke within 7 days of onset

• Sign informed consent, provide relevant medical history information and provide biological specimens

Locations
Other Locations
China
Nanfang Hospital,Southern Medical University
RECRUITING
Guangzhou
Contact Information
Primary
Jia Yin, M.D
jiajiayin@139.com
13802964883
Backup
Weike Hu, M.D
weike946@gmail.com
18326349212
Time Frame
Start Date: 2024-01-30
Estimated Completion Date: 2028-12-31
Participants
Target number of participants: 400
Treatments
modeling queue
The modeling queue is used to manage and prioritize tasks related to the development and training of models.
validation queue
The validation queue is designed to handle tasks related to the evaluation and validation of models.
Related Therapeutic Areas
Sponsors
Leads: Nanfang Hospital, Southern Medical University

This content was sourced from clinicaltrials.gov