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NCT07326410Not yet recruiting

Prevalence of Cerebral Large Vessel Occlusion Among Acute Ischemic Stroke Patients in Assiut University Hospitals

Source: ClinicalTrials.gov · Last updated 8 Jan 2026

Brief summary (registry, in English)

Prevalence of Large Vessel Occlusion among acute ischemic stroke patients in Assiut University hospitals 1. Study Objectives Primary Objective: \- To determine the prevalence of LVO among acute ischemic stroke (AIS) patients presenting to Assiut University hospitals Secondary Objectives: * To describe clinical and radiological characteristics of LVO patients. * To assess factors associated with LVO (age, sex, stroke severity, comorbidities). 2. Study Design * Type: single center, prospective observational cross-sectional study * Duration: 12-month recruitment period * Setting: Assiut university hospitals, stroke unit. 3. Study Population Inclusion Criteria: * Adults (≥18 years) * Diagnosed with acute ischemic stroke within 24 hours of symptom onset * Underwent vascular imaging (CTA or MRA) on admission Exclusion Criteria: * Hemorrhagic stroke * Stroke mimics * Incomplete imaging data 4. Definitions Large Vessel Occlusion (LVO) defined as occlusion in: * Intracranial ICA * M1 or proximal M2 segments of MCA * Basilar artery ± Optional: A1 6. Data Collection Clinical Data: * Demographics (age, sex) * Risk factors (HTN, DM, AF, CAD, smoking) * NIHSS on admission and discharge mRS on admission and discharge * Onset-to-door time * Imaging modality used Imaging Data: * Site of occlusion * ASPECTS (optional) * Collateral status (optional if available) Hospital Data: * Facility type (public vs private) * Door-to-CT and door-to-CTA times 8. Analysis Plan * Primary: Prevalence of LVO = Number of LVO cases / Total AIS patients with vascular imaging * Subgroup analysis: By age group, sex, region, NIHSS * Secondary: Logistic regression to identify predictors of LVO

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
8 Dec 2025
Start date
Feb 2026
Primary completion date
Feb 2027
Lead sponsor
Assiut University
Diseases
Stroke
NCT number
NCT07326410

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From Feb 2026 to the primary completion date, Feb 2027
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Hemorrhagic stroke
  • Stroke mimics

Other

  • Incomplete imaging data

Who the study is looking for

  • Adults (≥18 years)
  • Diagnosed with acute ischemic stroke within 24 hours of symptom onset
  • Underwent vascular imaging (CTA or MRA) on admission

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.