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Completed

NCT Number: NCT02483442

D-dimer Testing Tailored to Clinical Pretest Probability in Suspected Pulmonary Embolism

Prospective, multicentre, cohort study assessing a diagnostic management strategy for suspected Pulmonary Embolism with independent central adjudication of outcomes

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Alberta Hospital, Edmonton, Alberta, Canada

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About this study

This is a prospective, multi-centre, cohort study that will assess a new diagnostic management strategy for suspected Pulmonary Embolism (inpatients and outpatients). The new diagnostic strategy is designed to reduce the use of imaging tests for Pulmonary Embolism, particularly Computed Tomography Pulmonary Angiogram, by excluding Pulmonary Embolism with combinations of Clinical Pretest Probability and D-dimer results in a higher proportion of patients. The safety of this management strategy will be established by demonstrating a very low rate of proximal Deep Vein Thrombosis or Pulmonary Embolism during 90 days of follow-up in patients who had anticoagulant therapy withheld in response to negative diagnostic testing. Diagnostic test utilization will be assessed. All clinical outcomes will be adjudicated by a central independent adjudication committee that will be blind to initial D-dimer measurements and patient management.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients (either outpatients or inpatients) with clinically suspected Pulmonary Embolism.

Exclusion criteria

  • Age less than 18 years.
  • Treated with full-dose anticoagulation for ≥ 24 hours before D-dimer was measured.
  • Major surgery (general or spinal anesthesia) in the past 21 days.
  • Result of the D-dimer assay that will be used to manage the patient in the study is known before Clinical Pretest Probability was done.
  • Computed Tomography Pulmonary Angiogram or Ventilation Perfusion Scan was performed:
  • before Clinical Pretest Probability was documented, or
  • in a patient with Low Clinical Pretest Probability and a D-dimer level <1,000 ug/L (or equivalent), or
  • in a patient with Moderate Clinical Pretest Probability and a D-dimer level <500 ug/L (or equivalent).
  • Computed Tomography of the chest with contrast will be performed for another reason (e.g. to assess for malignant disease or aortic dissection), and would be performed even if Pulmonary Embolism is excluded by Clinical Pretest Probability and D-dimer testing.
  • Ongoing need for anticoagulant therapy.
  • Life expectancy less than 3 months.
  • Geographic inaccessibility which precludes follow-up.
  • Known pregnancy.
  • Inability to provide informed consent.

Treatment and study plan

Primary outcomes

  1. Number of patients with confirmed symptomatic proximal Deep Vein Thrombosis or Pulmonary Embolism

    Time frame: 90 Days (+ or - 7days)

    Proximal Deep Vein Thrombosis includes thrombosis confined to the calf vein trifurcation but not isolated more distal Deep Vein Thrombosis. Pulmonary Embolism does not include isolated sub-segmental abnormalities on Computed Tomography Pulmonary Angiography.

Secondary outcomes

  1. Number of patients with bleeding

    Time frame: 90 days (+ or - 7days)

    Major and minor bleeding

  2. Number of patient Deaths

    Time frame: 90 days (+ or - 7days)

    All deaths and cause specific deaths

  3. Number of patients with Venous Thromboembolism

    Time frame: 90 days (+ or - 7days)

    Venous Thromboembolism, including events that do not satisfy the primary outcome (e.g. isolated distal Deep Vein Thrombosis or subsegmental Pulmonary Embolism) but that are confirmed by the adjudication committee.

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)

Registry information

Official study title

D-dimer Testing,Tailored to Clinical Pretest Probability to Reduce the Use of CT Pulmonary Angiography in Suspected Pulmonary Embolism: A Management Study (The Pulmonary Embolism Graduated D-dimer [PEGeD] Study)

Acronym: PEGeD

Important dates

Study start
2015
Primary completion
2019
Study completion
2019
First posted
Jun 29, 2015
Registry last updated
Feb 6, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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