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Clinical Trial Summary

Patients receiving oral anticoagulation or anti-platelet therapy are at high risk of hematoma after device implantation. This study intends to examine the efficacy of the TopClosure(c) System in wound healing in these patients.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01665963
Study type Interventional
Source Hillel Yaffe Medical Center
Contact Mark Kazatsker, MD
Phone 972-4-6304656
Email markk@hy.health.gov.il
Status Not yet recruiting
Phase N/A
Start date September 2012
Completion date September 2013

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