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NCT06186024

A PROSPECTIVE, MULTICENTER, SINGLE-ARM TRIAL FOR THE NEW SIZES OF BRIDGE STENTS FOR VERTEBRAL ARTERY STENOSIS: Bridge-MAX

Status unknown NA Last updated 29 December 2023
What this trial tests

NA trial testing Bridge in Brain Diseases in 36 participants. Status unknown.

Timeline
27 September 2023
Primary endpoint
30 July 2024
30 January 2025

Quick facts

Lead sponsorMicroPort NeuroTech Co., Ltd.
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment36
Start date27 September 2023
Primary completion30 July 2024
Estimated completion30 January 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

MicroPort NeuroTech Co., Ltd.

Who can join

Adults 18 to 80, any sex, with Brain Diseases or Vertebral Artery Thrombosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Aprospective, multicentre, single-arm clinical trial in which approximately 36 subjects would be enrolled using the Bridge 4.5 mm and 5.0 mm stent in accordance with the inclusion and exclusion criteria in this protocol. The success rate of immediate post-procedure stent target lesion treatment was recorded for all subjects, and the incidence of in-stent restenosis (≥50% stenosis) was assessed by DSA imaging follow-up at 6 months (±30 days) post-procedure. The subjects were also followed up at 30 days (±7 days), 6 months (±30 days), and 12 months (±60 days) after stent implantation to assess safety events during the follow-up period. .

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Brain Diseases

Currently open trials in the same condition.

Other MicroPort NeuroTech Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

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/NCT06186024.

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