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N/A Completed N=452

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

Peripheral Vascular Diseases · Thrombosis · venous thrombosis
Source: ClinicalTrials.gov NCT00778336 ↗
Enrolled (actual)
452
Serious AEs
1.8%
Results posted
Apr 2011
Primary outcomePrimary: Change From Baseline to Final Angiographic Results — 1.32; 1.37; 1.16; 1.89 Occlusion Index — p=<0.0001

Summary

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

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline to Final Angiographic Results
1.32; 1.37; 1.16; 1.89; 3.67; 3.67 <0.0001 sig
SECONDARY
Rethrombosis
17; 11; 14; 0
SECONDARY
Description of Treatments by Thrombotic Condition
70; 78; 68; 6; 121; 144

Eligibility Criteria

Inclusion Criteria

  • 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 Criteria

  • None
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00778336). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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