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CompletedNCT07750015FORECAST-PCUpdated Aug 6, 2026

Derivation and External Validation of the "FORECAST-PC" Prediction Scores

An observational study in Posterior Ischemic Stroke, Cerebral Infarction and Cerebrovascular Disorders, sponsored by Dr. med. Alexander Salerno, MD-PhD. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-06.

Sponsored by Dr. med. Alexander Salerno, MD-PhD · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
732
Ages
18 Years and older
Sex
All
01

Study summary

This study aims to develop and externally validate machine learning prediction models (FORECAST-PC) to determine 90-day functional outcomes for patients suffering from acute ischemic stroke in the posterior circulation who are selected for endovascular thrombectomy (EVT)

Read the detailed description

Outcome prediction after endovascular treatment (EVT) for posterior circulation (PC) acute ischemic stroke remains challenging, as current prognostic tools are often limited strictly to basilar artery occlusions or rely heavily on anterior circulation data. The FORECAST-PC study is an investigator-initiated, retrospective, international multicenter cohort study designed to develop and validate comprehensive PC outcome prediction models across key stages of the clinical pathway: Baseline, Pre-EVT, Immediately Post-EVT, and 24-hours Post-EVT. The models are derived from patients across three European centers and externally validated on an unseen cohort from 11 international centers to ensure robustness against geographic domain shifts and variations in clinical workflows. The clinical utility of these models is assessed using Decision Curve Analysis to demonstrate the net benefit of model-guided prognostication over standard clinical assumptions.

02

Conditions studied

  • Posterior Ischemic Stroke
  • Cerebral Infarction
  • Cerebrovascular Disorders

Keywords

  • Machine Learning
  • Posterior Cerebral Artery
  • Basilar Artery
  • Vertebral Artery
  • Endovasculat treatment
  • Thrombectomy
  • Prediction Algorithm
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In context

Cerebral Infarction

219 studies on the registry are indexed under Cerebral Infarction; 46 are open to participants now.

This study's enrollment of 732 is above the median of 335 across 72 observational studies indexed under Cerebral Infarction.

Browse Cerebral Infarction studies →

Lead sponsor

This is the only study on the registry with Dr. med. Alexander Salerno, MD-PhD as lead sponsor.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population comprises adult patients (older than 18 years) presenting with acute ischemic stroke (AIS) attributed to a radiologically confirmed posterior circulation large vessel occlusion. These individuals were treated at 14 international comprehensive stroke centers, with initial participation rooted in the European EVA-TRISP network. Patients were included if they were selected for endovascular thrombectomy (EVT) within 24 hours of the last known well time, regardless of whether they received prior intravenous thrombolysis (IVT) or were managed via mothership or drip-and-ship pathways. Participants were required to have a pre-stroke modified Rankin Scale (mRS) of 0 to 3. The cohort explicitly excludes patients whose strokes occurred in-hospital, patients treated beyond the 24-hour window, and patients treated prior to 2015.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age > 18 years
  • Presentation with acute ischemic stroke (AIS) attributed to a radiologically confirmed posterior circulation occlusion
  • Selected for Endovascular Thrombectomy (EVT) according to the treating physician
  • Pre-stroke modified Rankin Scale (mRS) 0-3
  • EVT initiated or attempted within 24-hours of the last known well (LKW) time
  • Includes cases with/without prior intravenous thrombolysis (IVT), mothership, and drip-and-ship pathways

Exclusion criteria

Exclusion Criteria:

  • EVT carried out beyond 24 hours from stroke onset
  • EVT performed secondarily after in-hospital worsening or stroke recurrence
  • In-hospital strokes (to avoid the confounding influence of prior systemic comorbidities and the acute event that necessitated initial admission)
  • Missing primary outcome data
  • Inconsistencies between descriptive dependence status and raw pre-stroke mRS
  • Stroke cases occurring prior to 2015 (to account for major changes in endovascular treatment techniques)
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
732 participants (actual)
Patient registry
No

Groups and cohorts

  • Derivation cohort

    Patients with PC stroke selected for EVT from three primary training centers (Lausanne University Hospital, Bern University Hospital, and Charité-Universitätsmedizin Berlin).

    Other: FORECAST-PC Prediction Models

  • External Validation Cohort

    Unseen patients with PC stroke selected for EVT from 11 independent, world-wide comprehensive stroke centers

    Other: FORECAST-PC Prediction Models

Interventions

  • OtherFORECAST-PC Prediction Models

    Application of machine learning gradient-boosted decision tree models (Full-Feature and Light versions) at admission and 24-hours to predict 90-day functional outcome.

06

What researchers measure

Primary outcomes

  1. Unfavorable Functional Outcome at 90 Days

    Defined as a dichotomized 90-day modified Rankin Scale (mRS) score of 3 to 6 (where 0-2 is favorable and 3-6 is unfavorable).

    Time frame: 90 days

07

Study locations

1 site
  • Centre Hospitalier Universitaire Vaudois
    Lausanne, 1010, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07750015
Lead sponsor
Dr. med. Alexander Salerno, MD-PhD
Responsible party
Dr. med. Alexander Salerno, MD-PhD (Dr. med., MD-PhD, MERc-PD, Centre Hospitalier Universitaire Vaudois) — Sponsor-investigator
First posted
Aug 6, 2026
Start date
Jan 1, 2015
Primary completion
Dec 31, 2024
Completion
Dec 31, 2024
Last update
Aug 6, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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