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Eligibility: 3e7bdffe13d5bf95ad2977af492f62e2 [RDF]

Label 3e7bdffe13d5bf95ad2977af492f62e2
Slug 3e7bdffe13d5bf95ad2977af492f62e2
Criteria Inclusion Criteria: - Patient is >18 years of age - Patient has been informed and understands the nature of the study and provides written Informed Consent approved by the appropriate Institutional Review Board prior to enrollment - Patient has been trained and understands the use of the 0-10 Visual Analogue Scale as an assessment of patient pain - Patient is scheduled to undergo a diagnostic endovascular procedure involving percutaneous access through the common femoral artery Exclusion Criteria: - Per Mynx and Angio-Seal Instructions for Use - Patient has a documented psychiatric disorder (e.g. major depression, anxiety) - Patient has a documented chronic pain condition requiring daily treatment - Patient carries the diagnoses of a known bleeding disorder - Intraprocedural Exclusion Criteria: Patient has a baseline ipsilateral groin pain rating of >1 on the 0-10 Visual Analog Scale prior to closure device deployment
Maximum age N/A
Healthy volunteers No
Study pop
Minimum age 18 Years
Gender Both
Sampling method
Provenances http://clinicaltrials.gov/show/NCT00998023?displayxml=true
Similars None
Interlinks None