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Pulmonary embolism diagnosis study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN65486961
Enrollment
1530
Registered
2005-09-26
Start date
2005-11-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Pulmonary embolism (PE) Circulatory System Pulmonary embolism (PE)

Interventions

Clinical model to identify PE likely or unlikely, Ddimer blood test, randomised to receive either V/Q or CT for diagnosis of possible PE, in majority of cases would have ultrasound to rule out deep ve

Sponsors

Queen Elizabeth II Health Science Centre (Nova Scotia) (Canada)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Consecutive adult patients (18 years and older) of either sex, presenting with symptoms or signs suspected by a physician of being caused by acute pulmonary embolism (acute onset of new or worsening shortness of breath, chest pain, hemoptysis, presyncope or syncope) will be potentially eligible for this study.

Exclusion criteria

Exclusion criteria: 1. Deep vein thrombosis or pulmonary embolism within the previous 3 months 2. No worsening of the severity of pulmonary symptoms within the previous 2 weeks 3. Use of therapeutic doses of parenteral anticoagulants for greater than 48 hours 4. Co-morbid condition making life expectancy less than 3 months 5. Contradiction to contrast media 6. A need for long-term use of anticoagulants 7. Pregnancy 8. Age less than 18 years 9. Refusal to give informed consent 10. Geographic inaccessibility to follow-up

Design outcomes

Primary

MeasureTime frame
Symptomatic venous thromboembolism.

Secondary

MeasureTime frame
1. Asymptomatic venous thromboembolism 2. Death 3. Bleed (major and minor)

Countries

Canada

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 6, 2026