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Zilver PTX Post-Market Study in Japan

Zilver PTX Post-Market Surveillance Study of Paclitaxel-Eluting Stents for Treating Femoropopliteal Artery Disease in Japan

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02254837
Enrollment
909
Registered
2014-10-02
Start date
2012-05-31
Completion date
2018-06-30
Last updated
2019-07-12

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

Conditions

Peripheral Arterial Disease (PAD)

Brief summary

Japanese post market clinical study of the Zilver PTX device.

Interventions

DEVICEZilver PTX Drug-Eluting Stent

Sponsors

Cook Group Incorporated
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Symptomatic peripheral arterial disease (PAD) involving the above-the-knee femoropopliteal arteries

Design outcomes

Primary

MeasureTime frame
Occurrence of stent fracture5 years
Rate of adverse events5 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 5, 2026