Skip to content

Prometheus Perfusion Study.

Prometheus perufsion study: Perfusion scanning in patients aged < or = 50 years with suspected pulmonary embolism - an accuracy study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20532
Enrollment
220
Registered
2010-02-08
Start date
2008-10-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Pulmonary embolism longembolie

Interventions

Perfusion scintigraphy, chest X-ray and CT scan in patients with likely or high clinical probablity and/or an abnormal D-dimer with suspected pulmonary embolism.

Sponsors

University Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: In- or outpatients aged < or = 50 years, with clinically suspected pulmonary embolism, who have a 'likely' (Wells score) or 'high' (revised Geneva score) clinical probability for pulmonary embolism and/or an abnormal D-dimer test and in hwom a cT scan will be made.

Exclusion criteria

Exclusion criteria: 1. Age 50 years; 2. Pregnancy; 3 (Low molecular weight) heparin for longer than 48 hours prior to eligibility assessment; 4. Inability to perfom a perfusion scan withing 24 hrs after CT scan; 5. Participation in a therapeutic study for pulmonary embolism is not an exclusion criterion.

Design outcomes

Primary

MeasureTime frame
The diagnostic accuracy of the perfsuion scan criteria in comparison to CT scan.

Secondary

MeasureTime frame
1. Positive predictive value; 2. Negative predictive value; 3. Proportion of diagnostic Q scans.

Contacts

Public ContactP.W. Kamphuisen

Meibergdreef 9

p.w.kamphuisen@amc.uva.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)