Status:

COMPLETED

A Prospective Observational Registry of Peripheral Use of AngioJet Rheolytic Thrombectomy With Mid-Length Catheters

Lead Sponsor:

Boston Scientific Corporation

Conditions:

Peripheral Vascular Diseases

Thrombosis

Eligibility:

All Genders

Brief Summary

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

Detailed 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, includin...

Eligibility Criteria

Inclusion

  • Patient has been treated with a mid-length AngioJet catheter(defined as 90-120 cm in length)
  • Patient has provided appropriate authorization per institutional policy and procedure.

Exclusion

  • None

Key Trial Info

Start Date :

January 1 2007

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

April 1 2010

Estimated Enrollment :

452 Patients enrolled

Trial Details

Trial ID

NCT00778336

Start Date

January 1 2007

End Date

April 1 2010

Last Update

October 17 2014

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