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A proof-of-concept study to evaluate 99mTechnetium radiolabeled Fucoidan as a diagnostic modality for thrombosis

Conditions
Deep vein thrombosis
Registration Number
NL-OMON26785
Lead Sponsor
one
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
12
Inclusion Criteria

Adult subjects of either gender, aged 50 years or older, with a compression ultra-sound demonstrated acute DVT, < 24 hours after treatment initiation
BMI between 18 and 35 kg/m2

Exclusion Criteria

Standard contra-indications to SPECT
Any medical condition or treatment that could interfere with the conduct of the study in the opinion of the investigator
Inability or unwilling to comply with protocol requirements, or deemed by the investigator to have a disorder that may compromise the ability to give informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The difference in uptake value of 99mTc-Fucoidan in the affected vein versus the corresponding vein in the unaffected leg of patients with an acute DVT
Secondary Outcome Measures
NameTimeMethod
To assess the effect of of Fucoidan on monocyte–endothelial and monocyte-platelet interaction in stimulated endothelium ex vivo
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