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Taking people in NorwayNo phase

Introducing clot removal treatment for acute ischemic stroke at a regional hospital

Studies a training-based quality program as a hospital starts treating strokes with clot removal.

Plain-language title generated from the registry record
Registry title: Establishing Mechanical Thrombectomy at a Limited-volume Stroke Center - Effects on Patient Morbidity and Mortality

Key facts

Where
Kristiansand, NorwaySee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 100 years old?

Source: NCT04942041, who can take part

Where in Norway

  • Sørlandet Hospital Health TrustKristiansand, NorwayTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Sorlandet Hospital HF
Trial code
NCT04942041
Record updated
29 December 2023
Original description
The regional health authorities of South-East Norway has commissioned Sørlandet Hospital (SSHF), Norway to establish mechanical thrombectomy in large-vessel occlusion stroke. SSHF is a limited volume stroke center, and introduction of thrombectomy may impose quality challenges. Therefore the implementation will be guided by a simulation based quality assurance program. In this study, we will monitor timelines, technical and clinical outcomes, including adverse events.Read full original descriptionShow less

Establishing Mechanical Thrombectomy at a Limited-volume Stroke Center - Effects on Patient Morbidity and Mortality.

The regional health authorities of South-East Norway has commissioned Sørlandet Hospital (SSHF), Norway to establish mechanical thrombectomy in large-vessel occlusion stroke. SSHF is a limited volume stroke center, and introduction of thrombectomy may impose quality challenges. Therefore the implementation will be guided by a simulation based quality assurance program. In this study, we will monitor timelines, technical and clinical outcomes, including adverse events.

Inclusion: Adult patients; Large vessel occlusion stroke.

Exclusion: Intracranial hemorrhage, tumor, aneurism or vascular malformation i the stroke area; More than 24 hours after stroke onset.

ClinicalTrials.gov NCT04942041