Antares Coronary Stent System to Facilitate Side Branch Interventions

Treatment sucess with the Antares Stent System for Coronary Artery Stenting at or near a Major Sidebranch

Status

Terminated

Phases

Unknown

Study type

Interventional

Source

ANZCTR

Registry ID

ACTRN12609000487213

Acronym

TOP II

Enrollment

Registered

2009-06-18

Start date

2009-07-15

Completion date

2009-08-31

Last updated

2020-01-13

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

Conditions

None listed

Brief summary

Study to evalute the use of the Antares Stent System in patients with coronary disease at a location where two vessels are meeting.

Interventions

Coronary Stenting involves placing a metal mesh in a blood vessel in the heart to open a blockage. The stent is inserted through a blood vessel in the arm or leg and is put in place by inflating a balloon inside the stent. The stent cannot be removed from the blood vessel once it is in place.

Study design

Allocation

Non-randomised trial

Intervention model

Single group

Primary purpose

Treatment

Masking

Open (masking not used)

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Healthy volunteers

Inclusion criteria

symptomatic or documented myocardial ischemia, study lesion is a single bifurcation lesion that has not been previously treated, By angiograpic review the study lesion has a diameter and length appropriate for Antares Stent,

Exclusion criteria

Acute myocardial infarction, Shock, Stroke, Coagulopathy, Left main coronary lesion, Total occlusion, Diffuse disease, thrombus or severe calcification, Previous Coronary Artery Bypass Graft (CABG) surgery,

Outcome results