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Diagnostic management of acute upper extremity thrombosis with Magnetic Resonance Direct Thrombus Imaging

Diagnostic management of acute upper extremity thrombosis with Magnetic Resonance Direct Thrombus Imaging - MRDTI of the upper extremity veins

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON36551
Enrollment
144
Registered
2011-05-26
Start date
2012-01-25
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

arm thrombosis upper extremity thrombosis

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: All patients with a suspected UE-DVT are eligible for inclusion. Patients are at least 18 years of age and able and willing to provide informed consent.

Exclusion criteria

Exclusion criteria: Patients are excluded if the duration of the complaints lasted more than 10 days, if they have a MRI contra-indication, if it is impossible to perform MRDTI within 48 hours. Patients with upper-limb amputation and those with a medical condition, associated illness, or co-morbid circumstances that made it unlikely that the study procedure would be completed are also excluded.

Design outcomes

Primary

MeasureTime frame
The primary study parameters are the sensitivity and specificity of MRDTI for diagnosing acute arm vein thrombosis. The sensitivity of MRDTI is determined by calculating te proportion of scans that are read as "positive for acute arm vein thrombosis" and the specificity is determined by calculating the proportion of scans that are read as "negative for acute arm vein thrombosis".

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)