Actively Recruiting

Age: 18Years - 90Years
All Genders
ID04230785

Clinical Significance of Circulating Non-coding RNA in Acute Ischemic Stroke With Endovascular Treatment (EVTRNA)

Led by Nanjing First Hospital, Nanjing Medical University · Updated on 2026-04-09

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

N

Nanjing First Hospital, Nanjing Medical University

Lead Sponsor

Z

Zhongda Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research focuses on acute ischemic stroke patients undergoing endovascular treatment. It aims to study the patterns of certain non-coding RNAs—circular RNA, long non-coding RNA, and micro-RNA—before and after treatment. These RNA types are being explored as potential biomarkers and regulators for stroke progression and prognosis, as well as their impact on the immune system following stroke. The study observes two groups of patients: those before and those after endovascular treatment. It uses advanced genetic techniques like next-generation sequencing and quantitative real-time polymerase chain reaction to analyze the RNA expression. Researchers will identify specific RNA patterns and develop a predictive model to relate these findings to immune status and stroke outcomes. Participants will have their RNA levels measured and monitored for 90 days to assess changes over time. The study also examines the relationship between these RNAs and inflammatory factors, stroke-associated infections, and overall prognosis. This observational study does not involve experimental treatments but collects detailed biological data to better understand stroke recovery and treatment effects.

CONDITIONS

Brief Title

Circulating Non-coding RNA in Acute Ischemic Stroke With Endovascular Treatment (EVTRNA)

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18 years or older
  • Confirmed acute ischemic stroke by diffusion-weighted MRI and brain CT scan
  • Within 24 hours of symptom onset and receiving endovascular therapy
  • Good performance status
  • Signed an approved informed consent
Not Eligible

You will not qualify if you...

  • History of hemorrhagic infarction
  • Chronic kidney or liver diseases
  • Peripheral arterial occlusive disease
  • Active malignant disease
  • Inflammatory or infectious diseases

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Within 24 hours of symptom onset

Participants undergo assessments including diffusion-weighted MRI and brain CT scan to confirm acute ischemic stroke.

1 visit (in-person)

Monitoring

Duration - Up to 90 days

Participants are observed to evaluate the expression patterns of non-coding RNA before and after endovascular treatment.

Multiple visits during the 90-day follow-up period

Trial Site Locations

Total: 1 location

1

Nanjing First Hospital, Nanjing Medical University

Nanjing, Jiangsu, China, 210006

Actively Recruiting

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Research Team

J

Junshan Zhou, M.D

Q

Qiwen Deng, M.D

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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