Posterior Circulation Clot Burden Score (Pc-CBS) Predicts Clinical Outcome After Acute Ischemic Stroke Related to Posterior Circulation Occlusions : An Externally Validated Radiological Score

NCT07122934 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1828

Last updated 2025-08-14

No results posted yet for this study

Summary

Posterior circulation strokes (PCS) represent \~30% of all ischemic strokes, but existing prognostic tools are limited, especially for non-basilar artery occlusions. Accurate early outcome prediction may aid treatment decisions and clinical trial design. We developed and externally validated the Posterior Circulation Clot Burden Score (PC-CBS), a radiological tool to predict 3-month functional outcome in acute ischemic stroke due to posterior circulation occlusion.

Conditions

  • Acute Ischemic Stroke
  • Posterior Circulation Brain Infarction
  • Arterial Occlusion Disease

Interventions

DIAGNOSTIC_TEST

Assessment of cervico-cerebral arterial occlusion pattern

Assessment of cervico-cerebral arterial occlusion pattern for the development of a radiological score

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    collaborator OTHER
  • Hospital de Egas Moniz

    collaborator OTHER
  • University Hospital Heidelberg

    collaborator OTHER
  • IRCCS Istituto delle Scienze Neurologiche di Bologna

    collaborator OTHER
  • The University of Texas Health Science Center, Houston

    collaborator OTHER
  • Azienda Ospedaliero-Universitaria di Modena

    collaborator OTHER
  • Hospital Vall d'Hebron

    collaborator OTHER
  • Boston University

    collaborator OTHER
  • Università degli Studi di Brescia

    collaborator OTHER
  • Medical University of Graz

    collaborator OTHER
  • Hôpital Rothschild

    collaborator OTHER
  • Medical University of Vienna

    collaborator OTHER
  • Hebrew University of Jerusalem

    collaborator OTHER
  • Michigan State University

    collaborator OTHER
  • Medical University Innsbruck

    collaborator OTHER
  • Ludwig-Maximilians - University of Munich

    collaborator OTHER
  • Ospedale Policlinico San Martino

    collaborator OTHER
  • EOC Lugano CH

    collaborator UNKNOWN
  • University Hospital, Basel, Switzerland

    collaborator OTHER
  • Aristotle University Of Thessaloniki

    collaborator OTHER
  • Technische Universität Dresden

    collaborator OTHER
  • Centre Hospitalier Universitaire Vaudois

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-02-01
Primary Completion
2023-03-31
Completion
2025-08-08

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07122934 on ClinicalTrials.gov