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NCT02328781: PESS

Prospective Evaluation of Safety and Efficacy Vertebral Drug-eluting Stent System

Completed NA Last updated 12 June 2020
What this trial tests

NA trial testing Drug-eluting stent in Vertebrobasilar Insufficiency in 101 participants. Completed in 25 November 2016.

Timeline
17 July 2014
Primary endpoint
14 June 2016
25 November 2016

Quick facts

Lead sponsorZhongrong Miao
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment101
Start date17 July 2014
Primary completion14 June 2016
Estimated completion25 November 2016
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Zhongrong Miao

Who can join

Adults 18 to 80, any sex, with Vertebrobasilar Insufficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate the safety and efficacy of Firehorus vertebral artery rapamycin-target-eluting stent system (hereinafter referred to as Firehorus) in treatment of symptomatic vertebral artery stenosis.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of Drug-eluting stent

Trials testing the same drug.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing