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Clinical Trials/NCT05906420
NCT05906420Active, not recruitingNot Applicable

Pc-ASTRAL Score for the Prediction of 3 Months Functional Outcome in Acute Ischemic Stroke at the Posterior Circulation

University of Thessaly2 sites in 2 countries2,000 target enrollmentStarted: January 1, 2003Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
2,000
Locations
2
Primary Endpoint
3 months modified Ranking scale

Study Overview

Brief Summary

The goal of this study is to develop a prognostic score for ischemic posterior circulation strokes, based on our previous work on with the ASTRAL scores (Acute STroke Registry and Analysis of Lausanne) on overall stroke prognosis, intracranial occlusion, recanalization and stroke recurrences. The main question it aims to answer is the modified Rankin score in 3 months after the event.

Participants will be patients with acute ischemic stroke of the posterior circulation with mRS priot to event <3. All the data will be collected retrospectively from patients included in the ASTRAL registry between January 2003 and December 2021. The ASTRAL registry will be used as the derivation cohort of the score. Demographics, acute glucose, NIHSS score and acute imaging of each participant will be used from the derivation cohort in order to create an integer-based prognostic score. After internal validation, we plan to validate the score in external stroke registries to show its validity.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Isolated posterior circulation strokes based on clinical or/and imaging evidence.
  • Arriving within 24h at hospital since last proof of good health.

Exclusion Criteria

  • no available data for 3 months modified Rankin Score
  • modified Rankin Score≥3 prior the event

Outcomes

Primary Outcomes

3 months modified Ranking scale

Time Frame: January 2003-December 2021

evaluation of 3 months neurological disability

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

George Ntaios

Professor of Internal Medicine George Ntaios

Aristotle University Of Thessaloniki

Study Sites (2)

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