CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 296 enrolled
Drug / intervention
COBRA PzFdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01925794
NCT01925794N/ACompleted

COBRA PZF™ Coronary Stent System in Native Coronary Arteries for Early Healing, Thrombus Inhibition, Endothelialization and Avoiding Long-Term Dual Anti-Platelet Therapy. The PzF Shield Trial

CeloNova BioSciences, Inc.·interventional·Posted Aug 20, 2013·Updated Dec 22, 2021

In Brief

A clinical study evaluating COBRA PzF for Coronary Artery Disease. Completed, enrolled 296 participants across 35 sites in 7 countries.

Detailed Summary

This is a prospective, multi-center, non-randomized, single arm clinical trial that will be conducted at up to 40 sites in the United States and Outside United States (OUS). This study will enroll patients with symptomatic ischemic heart disease due to a single de novo lesion contained within a native coronary artery with reference vessel diameter between 2.5 mm and 4.0 mm and lesion length ≤ 24 mm that is amenable to percutaneous coronary intervention (PCI) and stent deployment. All patients will be followed at 30 days, 6 months, 9 months, 1 year and annually for 5 years post index stenting procedure.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesFrance, Germany, Latvia, Serbia, Spain, Switzerland, United States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedAug 20, 2013
Enrollment StartAug 21, 2013
Primary CompletionNov 1, 2015
Study CompletionMar 2, 2020
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 12.9 years ago

Interventions

COBRA PzFdevice