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Drug Coated Balloon Versus Stenting in Patients With Symptomatic Vertebral Artery Stenosis：an Observational Clinical Study

NCT03311360 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 95

Last updated 2021-08-03

No results posted yet for this study

Summary

There are two arms in our trial, DCB group, BMS group.The investigators are going to investigate the safety and efficacy of all groups at 6 months and 12 months.

Conditions

  • Vertebral Artery Origin Stenosis

Interventions

DEVICE

drug-coated balloon

Orchid and Dahlia DCB

DEVICE

bare metal stent

any type of bare metal stent

Sponsors & Collaborators

  • Chinese Society of Interventional Radiology

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2020-02-01
Completion
2020-10-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03311360 on ClinicalTrials.gov