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Clinical Trials/NCT06290076
NCT06290076
Completed
Not Applicable

A Predictive Model and Scoring System for Severe Complications After Endovascular Thrombectomy: a Retrospective, Multicenter, Observational Study

Xuanwu Hospital, Beijing1 site in 1 country1,500 target enrollmentJanuary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Ischemic Stroke
Sponsor
Xuanwu Hospital, Beijing
Enrollment
1500
Locations
1
Primary Endpoint
Rate of severe complications
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

To establish a predictive model and scoring system for predicting severe complications after thrombectomy. This scoring system can be used to identify high-risk patients after endovascular thrombectomy, guide the early use of adjunctive interventions, and provide reference for future clinical trials.

Detailed Description

Acute ischemic stroke (AIS) accounts for about 80% of all strokes. The focus of AIS treatment is to restore reperfusion of ischemic territory as soon as possible, promote neurological recovery, reduce disability rate and improve long-term survival rate. In recent years, a series of randomized clinical trials have proved that endovascular thrombectomy (EVT) is safe and effective in the treatment of anterior circulation AIS. EVT has been recommend as the first-line treatment for anterior circulation large vessel occlusion (LVO) stroke by guidelines. Symptomatic intracranial hemorrhage (sICH) and malignant cerebral edema (MCE) are the two most common severe neurological complications, leading to brain tissue hypoxia and neurological dysfunction. Currently, there is a lack of prediction system to identify patients at high risk for severe complications, who can most likely benefit from adjuvant treatment after thrombectomy to improve patient functional independence and survival rate.

Registry
clinicaltrials.gov
Start Date
January 1, 2020
End Date
September 30, 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Symptoms and signs compatible with ischemia in the anterior circulation
  • Internal carotid artery occlusion or middle cerebral artery M1 and M2 segment occlusion confirmed by computed tomographic angiography (CTA)/ magnetic resonance angiography (MRA)/ digital subtraction angiography (DSA)
  • Premorbid mRS ≤1;
  • National Institutes of Health Stroke Score (NIHSS) ≥6 at admission;
  • Onset to puncture time ≤24h;
  • Treated with thrombectomy resulting in mTICI score ≥2b at end of the procedure.

Exclusion Criteria

  • Intracranial hemorrhage, aneurysm, and arteriovenous malformation before endovascular thrombectomy;
  • Perioperative complications, including dissection and arterial perforation;
  • Anticipated life expectancy \<3 months;
  • Critical baseline clinical, laboratory and imaging data are missing;
  • Lack of follow-up results within 72 hours and 90 days after thrombectomy;
  • Pregnant or lactating women;
  • Severe systemic diseases (e.g. advanced cancer), potentially interfering with prognosis;
  • Allergy to contrast media and nitinol;
  • Concurrent participation in a study that would interfere with the establishment of predictive models;
  • Unable to complete the assessment due to mental disorders cognitive or emotional disorders before onset.

Outcomes

Primary Outcomes

Rate of severe complications

Time Frame: Within 72 hours after thrombectomy

Severe complications include symptomatic intracranial hemorrhage (sICH) and malignant cerebral edema (MCE). SICH was defined as any intracranial hemorrhage on the non-contrast CT scan accompanied with clinical deterioration, as defined by a increase of ≥4 points in the NIHSS score, or that led to death and that was identified as the predominant cause of the neurologic deterioration. MCE was defined as a malignant state in which neurological function deteriorates progressively due to brain edema after endovascular thrombectomy, causing disturbance of consciousness, anisocoria, and midline shift of 5 mm or more on imaging, leading to brain herniation or death. Midline shift was obtained by measuring the point of maximum deviation perpendicular to the line connecting the anterior and posterior attachment points of the falx cerebri.

Secondary Outcomes

  • Rate of symptomatic intracranial hemorrhage(Within 72 hours after thrombectomy)
  • Rate of modified Rankin Scale (mRS) score of 0-2(90 days (±7 days) after thrombectomy)
  • Rate of malignant cerebral edema(Within 72 hours after thrombectomy)
  • Rate of mRS score of 5-6(90 days (±7 days) after thrombectomy)
  • Change of NIHSS score(24-72 hours after thrombectomy versus admission)
  • All-cause mortality(90 days (±7 days) after thrombectomy)
  • Rate of mRS score of 3-6(90 days (±7 days) after thrombectomy)

Study Sites (1)

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