Xtract™ Aspiration Catheter Registry Study

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00349570

Enrollment

Unknown

Registered

2006-07-07

Start date

2006-08-31

Completion date

2008-03-31

Last updated

2008-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fresh Soft Emboli or Thrombi in the Arteries.

Keywords

thrombus, aspiration catheter

Brief summary

Intra-coronary thrombosis and thromboembolism continues to be a challenge for percutaneous coronary and other vascular interventional techniques. The Xtract™ Aspiration Catheter is a single use device designed to remove fresh, soft emboli and thrombi from the arterial system using standard catheter techniques, compatible with 6 Fr guide catheters and 0.014 guidewires. The purpose of this registry study is to validate the design and demonstrate the performance of the Xtract Aspiration Catheter as a thrombectomy catheter during percutaneous intervention of vessels in the arterial system. Subjects will be enrolled during percutaneous intervention when the Interventional Physician decides a thrombectomy catheter is needed to remove thrombus during the procedure.

Interventions

DEVICEXtract Aspiration Catheter

Study design

Allocation

NON_RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* Planned percutaneous intervention to a native coronary, coronary vein graft, renal artery or carotid artery lesion * Angiographic evidence of thrombus.

Design outcomes

Primary

Measure	Time frame
The primary objective of the study will be to evaluate the performance of the Xtract Aspiration Catheter.	—

Countries

New Zealand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026