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 |
