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Endovascular treatmenT for Acute Ischemic Stroke in China

Completed
Conditions
Endovascular Treatment
Stroke
Registration Number
NCT04752735
Lead Sponsor
General Hospital of Shenyang Military Region
Brief Summary

This is a retrospective real world registry study, aiming to explore the effectiveness and safety of endovascular treatment of acute ischemic stroke in a Chinese population.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1000
Inclusion Criteria
  • Age: ≥ 18;
  • Ischemic stroke confirmed by head CT or MRI;
  • Patients receiving endovascular treatment;
  • First ever stroke or mRS≤2 after previous disease;
  • Complete and clear pre- and post-operative DSA images are available
Exclusion Criteria
  • Imaging data not qualified for evaluation;
  • Absence of important clinical data;
  • The first 50 patients receiving endovascular treatment in a single centerr.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of patients with modified Rankin Score (mRS) 0 to 2Day 90

the minimum and maximum values of mRS are 0 and 6, respectively; higher mRS mean a worse outcome

Secondary Outcome Measures
NameTimeMethod
Proportion of intraparenchymal hemorrhage (PH1 and PH2)48 hours

Proportion of intraparenchymal hemorrhage (PH1 and PH2) after treatment

Proportion of patients with modified Rankin Score 0 to 2Day180, 360

Proportion of patients with modified Rankin Score 0 to 2

Proportion of symptomatic intracranial hemorrhage (sICH)48 hours

sICH was defined as 4 or more increase in NIHSS caused by hemorrhage

Proportion of deathDay 7

death due to any cause

Changes in National Institute of Health stroke scale (NIHSS)Day 2, 7, 14

the minimum and maximum values of NIHSS are 0 and 42, respectively; higher NIHSS mean a worse outcome

Distribution of modified Rankin ScoreDay 90, 180, 360

Distribution of modified Rankin Score after treatment

Changes in cerebral edema48 hours, 7 days

edema is determined by middle shift.

Trial Locations

Locations (1)

Department of Neurology, General Hospital of Northern Theater Command

🇨🇳

Shenyang, China

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