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Implementation of a Structured Post-pulmonary Embolism Follow-up Model

StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated June 13, 2025 (before its estimated March 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Primary endpoints: 1 to 2v4 Show 4 more changesShow less
    • Eligibility criteria expanded, about 9 words
    • Secondary endpoints: 7 to 10
    • Publications: 1 to 4
    • Study description expanded, about 2 words
  2. Study description revisedv3
  3. Primary completion date: Oct 2025 to Mar 2026
    • Study completion date: Oct 2025 to Oct 2026
    • Study description revised
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Venous thromboembolism (VTE), clinically presenting as deep vein thrombosis or pulmonary embolism (PE) is the third most frequent cardiovascular disease and is associated with substantial short- and long-term morbidity and mortality and high costs of care. In addition negative physical and mental complications following VTE are common. However in terms of PE, there are no structured follow-up programs in Denmark and there is considerable variation in practice patterns of post-PE management both within and between countries. This project aims to develop, test and implement a structured follow-up care model for patients with PE (The Attend-PE model). This project is a pre-post intervention study and will estimate the effectiveness of implementing the structured follow-up care model on a national level.
Trial Details
NCT Number NCT06037096
Lead Sponsor Aalborg University Hospital
Collaborators: Aarhus University Hospital
Conditions
(from sponsor)		 Pulmonary Embolism
Related terms Pulmonary Embolism
Enrollment 2,000 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov