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

N

Nanjing Medical University

Status

Enrolling

Conditions

Endovascular Treatment
Stroke, Acute
Stroke, Ischemic

Treatments

Genetic: Sequencing of circRNA/lncRNA/miRNA

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

EVTRNA is to analyze the differentiated expression pattern of circular RNA (circRNA), long non-coding RNA (lncRNA) and micro-RNA (miRNA) by next-generation sequencing in acute ischemic stroke patients before and/or after endovascular treatment. The candidate circRNA/lncRNA/miRNA will be verified as the biomarker and regulator for progression and prognosis of acute ischemic stroke with endovascular treatment. Further, the candidate non-coding RNA will be used to evaluate the effect of endovascular treatment on both peripheral and central immune after stroke.

Full description

Noncoding RNAs have been highlighted to be involved in the pathological process of ischemic stroke (IS). The purpose of this protocol will investigate the differentiated expression pattern of circular RNA (circRNA), long non-coding RNA (lncRNA) and micro-RNA (miRNA) by next-generation sequencing in acute ischemic stroke patients before and/or after endovascular treatment. The candidate circRNA/lncRNA/miRNA will be verified as the biomarker and regulator for progression and prognosis of acute ischemic stroke with endovascular treatment. Further, the candidate non-coding RNA will be used to evaluate the effect of endovascular treatment on both peripheral and central immune after stroke. Distinctive expression patterns of circRNA/miRNA/lncRNA will be identified by the next-generation sequencing and individual quantitative real time polymerase chain reaction (qRT-PCR). A predictive model will be established using logistic regression. The panel of these altered ncRNAs may be associated with the immune status after acute IS and could serve as a regulator for progression and prognosis of acute ischemic stroke with endovascular treatment.

Enrollment

300 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18 years or older
  • Confirmed acute ischemic stroke by a diffusion-weighted imaging-position lesion on magnetic resonance imaging (MRI) and a new lesion on a brain computed tomography (CT) scan
  • Within 24 hours of symptom onset and treat with endovascular therapy
  • Good performance status
  • Signed an approved informed consents

Exclusion criteria

  • a history of hemorrhagic infarction, chronic kidney/liver diseases, peripheral arterial occlusive disease, active malignant disease, and inflammatory or infectious diseases

Trial design

300 participants in 2 patient groups

AIS before EVT group
Description:
This group includes patients with acute ischemic stroke (AIS) before endovascular treatment (EVT)
Treatment:
Genetic: Sequencing of circRNA/lncRNA/miRNA
AIS after EVT group
Description:
This group includes patients with acute ischemic stroke (AIS) after endovascular treatment (EVT)
Treatment:
Genetic: Sequencing of circRNA/lncRNA/miRNA

Trial contacts and locations

1

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Central trial contact

Junshan Zhou, M.D; Qiwen Deng, M.D

Data sourced from clinicaltrials.gov

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