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NCT01628159 · ClinicalTrials.gov registry record · NA

LEVANT 2 Continuation Registry of the Lutonix® Drug Coated Balloon (DCB)

A NA study, sponsored by C. R. Bard.

Completed
Registry status
NA
Development phase
657
Enrollment target

NCT01628159: Completed NA study, sponsored by C. R. Bard.

NCT01628159 is a NA study that has completed, run by C. R. Bard. The registered enrollment target is 657 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (53% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01628159, a NA study, has completed, sponsored by C. R. Bard.

COMPLETED
Registry status
NA
Development phase
657 participants
Enrollment target

Study Summary

The purpose of the study is to collect additional safety and efficacy information on the Lutonix (formerly Moxy) Drug Coated Balloon for treatment of stenosis or occlusion of the femoral and popliteal arteries.

Interventions

  • DEVICE Lutonix Drug Coated Balloon

Trial Details

FieldValue
Enrollment Target 657 participants
Start Date 2012-06
Est. Completion 2018-12
Phase NA
C. R. Bard

75 total trials

What the finished NCT01628159 record still lists

NCT01628159 is an interventional study that assigns participants to a tested intervention. The registered 657 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (53% lower).

The record links to 0 conditions, and to 1 intervention - of which Lutonix Drug Coated Balloon is the first listed.

NCT01628159 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01628159 about?

NCT01628159 is a clinical study titled "LEVANT 2 Continuation Registry of the Lutonix® Drug Coated Balloon (DCB)". The purpose of the study is to collect additional safety and efficacy information on the Lutonix (formerly Moxy) Drug Coated Balloon for treatment of stenosis or occlusion of the femoral and popliteal arteries.

What is the current status of trial NCT01628159?

This trial is currently completed. It is a NA study. The enrollment target is 657 participants. The study started on 2012-06. Estimated completion is 2018-12.

What interventions are being tested in trial NCT01628159?

The interventions under investigation include: Lutonix Drug Coated Balloon (DEVICE).

Who is sponsoring clinical trial NCT01628159?

This trial is sponsored by C. R. Bard, which has 75 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01628159's enrollment target sits among peer trials

657 156th of 2000 higher than 1,845 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01628159, the US trial registry maintained by the National Library of Medicine. NCT01628159 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.