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NCT03737162: BASELINE

Bare-metal Stent vs Covered Stent in Chinese Patients With Subclavian Occlusive Lesions

Status unknown NA Last updated 9 November 2018
What this trial tests

NA trial testing Stent implantation of subclavian artery in Subclavian Occlusion in 408 participants. Status unknown.

Timeline
2 April 2018
Primary endpoint
3 April 2020
3 July 2020

Quick facts

Lead sponsorXuanwu Hospital, Beijing
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment408
Start date2 April 2018
Primary completion3 April 2020
Estimated completion3 July 2020
Sites6 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Xuanwu Hospital, Beijing

Who can join

50 and older, any sex, with Subclavian Occlusion. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Bare-metal stent vs Covered stent with subclavian occlusive lesions to verify the efficacy and safety.Study Design are prospective, multiple center, randomized, open, positive controlled, non-inferiority trail.Case total numbers enrollment predict 408 cases,each group 204 cases.Follow up period for 1 years.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Xuanwu Hospital, Beijing trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03737162.

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