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Clinical Trial Summary

This registry collects observational data about how mid-length AngioJet catheters (ie XPEEDIOR and DVX models) are used in routine clinical practice.


Clinical Trial Description

The PEARL Registry collects real world data about mid-length AngioJet catheters to:

- Characterize usage patterns, treatment approaches, and targeted vessels

- Document treatment strategies, including specific techniques and concomitant therapies

- Collect outcome data during initial hospitalization and at a 3-month follow-up phone call or visit

- Evaluate the frequency of specific clinical events in relation to risk factors, diagnosis, and treatments provided

- Identify treatment strategies that may optimize procedural and clinical outcomes, to facilitate development of treatment guidelines

- Offer sites a valuable resource for tracking usage and performance of the AngioJet System at their institution

Information collected by the PEARL Registry is intended for educational and clinical research purposes only. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00778336
Study type Observational
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date January 2007
Completion date April 2010

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