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NCT06453252 Clinical Trial

Predictors of Intracranial Atherosclerotic Disease in Posterior Circulation: a Cohort Study

Stroke, Ischemic Clinical Trial

Official title:
Predictors of Intracranial Atherosclerotic Disease in Posterior Circulation: a Cohort Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06453252
Other study ID # Soh-Med-24-05-04MD
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 15, 2024
Est. completion date June 30, 2026

Study information
Verified date June 2024
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Early identification of intracranial atherosclerotic disease (ICAD) may impact the management of patients undergoing mechanical thrombectomy (MT). The aim of the study is to develop and validate a scoring system for pre-thrombectomy diagnosis of ICAD in posterior circulation large vessel/distal medium vessel occlusion strokes (LVOs/DMVOs).

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 150
Est. completion date June 30, 2026
Est. primary completion date June 1, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Adult =18 years 2. Patient with posterior circulation strokes who underwent mechanical thrombectomy. Exclusion Criteria: 1. Patients with anterior circulation stroke. 2. Patients with intracranial hemorrhage 3. Patients without baseline radiological data. 4. Extracranial large vessel atherosclerosis related strokes.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• we are aiming to develop a Scoring system based on certain variables derived from both groups
We are aiming to develop a Scoring system based on certain variables derived from both group

Locations
Country Name City State
Egypt Sohag university hospitals Sohag
United States Marcus stroke and neuroscience center, Grady Memorial Hospital Atlanta Georgia

Sponsors (2)
Lead Sponsor Collaborator
Sohag University Emory University

Countries where clinical trial is conducted

United States,  Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Post-procedural outcomes included any intracranial hemorrhage, symptomatic ICH (sICH) sICH is defined as local or remote parenchymal hemorrhage type 2, subarachnoid hemorrhage, and/or intraventricular hemorrhage, combined with a neurological deterioration of 4 points or more on the NIHSS from baseline or leading to death that the physician judged was causative of the deterioration) per ECASS III criteria June 1st, 2025
Secondary 90 day modified Rankin scale (mRS) a score of 0 to 4 on the modified Rankin scale (range, 0 to 6, with a score of 0 indicating no disability, 4 moderately severe disability, and 6 death) at 90 days, was changed to a good functional status (a modified Rankin scale score of 0 to 3, with a score of 3 indicating moderate disability) June 1st, 2025
Secondary 90 day mortality June 1st, 2025
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