Skip to content

Best Revascularisation Approach for Posterior Circulation Strokes With Isolated Vertebral Artery Occlusions

Best Revascularisation Approach for Posterior Circulation Strokes With Isolated Vertebral : the BRAVO Retrospective Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05503212
Acronym
BRAVO
Enrollment
682
Registered
2022-08-16
Start date
2003-01-01
Completion date
2023-08-09
Last updated
2023-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke, Vertebral Artery Ischemia, Arterial Occlusive Diseases, Vertebrobasilar Insufficiency

Keywords

Prognosis, Revascularization, Treatment

Brief summary

Isolated vertebral artery occlusions (VAO) account for approximately one third of posterior circulation occlusions, but have been given the least attention among posterior circulation strokes. If the two recent ATTENTION and BAOCHE randomized clinical trials have proven the superiority of endovascular thrombectomy (EVT) in basilar artery occlusions, data on the effectiveness and harm of acute revascularization treatment on isolated VAO is scarce. We aim to investigate the impact of acute recanalisation treatments in acute ischemic stroke patients with isolated VAO. In the absence of RCT, observational data with appropriate statistical methods may give indications on benefits and harms of treating neglected stroke situations like acute vertebral occlusion. Results may also lay the basis for prospective studies, such as randomized clinical trials.

Interventions

Best medical treatment without intravenous thrombolysis nor endovascular thrombectomy

OTHERIntravenous thrombolysis (IVT)

Best medical treatment with intravenous thrombolysis but without endovascular thrombectomy

OTHEREndovascular thrombectomy (EVT) ± intravenous thrombolysis (IVT)

Best medical treatment with endovascular thrombectomy with or without intravenous thrombolysis

Sponsors

Asan Medical Center
CollaboratorOTHER
St John of God Hospital, Vienna
CollaboratorOTHER
Medical University Innsbruck
CollaboratorOTHER
Hospital Vall d'Hebron
CollaboratorOTHER
University Hospital, Basel, Switzerland
CollaboratorOTHER
Clinical Centre of Serbia
CollaboratorOTHER
Charite University, Berlin, Germany
CollaboratorOTHER
Insel Gruppe AG, University Hospital Bern
CollaboratorOTHER
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
CollaboratorOTHER
Boston Medical Center
CollaboratorOTHER
Università degli Studi di Brescia
CollaboratorOTHER
The Cooper Health System
CollaboratorOTHER
University Hospital Carl Gustav Carus
CollaboratorOTHER
Duke University
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
Hadassah Medical Organization
CollaboratorOTHER
Sahlgrenska University Hospital
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
CollaboratorOTHER
Helsinki University Central Hospital
CollaboratorOTHER
The University of Texas Health Science Center, Houston
CollaboratorOTHER
University Hospital, Lille
CollaboratorOTHER
Hospital de Egas Moniz
CollaboratorOTHER
Neurocenter of Southern Switzerland
CollaboratorOTHER
Corewell Health West
CollaboratorOTHER
Azienda Ospedaliero-Universitaria di Modena
CollaboratorOTHER
Ludwig-Maximilians - University of Munich
CollaboratorOTHER
Azienda USL Reggio Emilia - IRCCS
CollaboratorOTHER_GOV
University of Zurich
CollaboratorOTHER
Centre Hospitalier Universitaire Vaudois
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute ischemic stroke limited to the posterior circulation * Presence of uni- or bilateral VAO (intracranial and/or extracranial) on at least one initial imaging study (CTA, MRA, DSA) * IVT, EVT or bridging-treated stroke patients between 01.01.2003 and 31.12.2021 * ≥ 18 years old

Exclusion criteria

* Extension of the occlusion into the basilar artery * Presence of a more distal occlusion in the pc (tandem occlusion/multilevel poster circulation occlusions) * Previously known chronic occlusion of the any segment of the vertebral artery/arteries * Local ethical/legal conditions in participating center not fulfilled

Design outcomes

Primary

MeasureTime frameDescription
3-month modified Rankin scale90 days3-month functional outcome, \[range: 0-6, 0= no symptoms, 6=death\]

Secondary

MeasureTime frameDescription
EVT procedural complicationsDuring EVT procedure or peri-proceduralAny complication attributed to the procedure (vessel perforation, vasospasm, dissection, Subarachnoid haemorrhage (SAH)/Intracerebral haemorrhage (ICH), device detachment/misplacement, embolization to new territory, access-site complications, early reocclusion, other)
24-hour NIHSS24 hoursNIH Stroke Scale/Score (NIHSS). Quantifies stroke severity based on weighted clinical evaluation findings at 24h. \[0-42, 0= no deficit, 42=maximum stroke severity\]
Early neurological deterioration (ENDi)24 hoursEarly neurological deterioration of ischemic origin (ENDi) is defined as an increase in National Institute of Health Stroke (NIHSS) score ≥ 4 points or death within 24 hours. \[yes/no\]
Symptomatic intracerebral haemorrhage (sICH)7 daysAny hemorrhagic transformation temporally related to any worsening in neurological condition. \[yes/no\]
24h and 3month mortality24h and 90 daysMortality at 24h and 3 months
Vessel recanalisation on follow up-imaging48 hoursVessel recanalisation at follow-up imaging (0= no recanalisation, 1= partial recanalisation 50-99%, 2=full recanalisation, 3= initially not occluded)
Cerebrovascular ischemic recurrences90 daysAny ischemic stroke or transient ischemic attack recurrence \[yes/no\]

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026