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Efficacy and Safety of a New Balloon Microcatheter in the Treatment of Intracranial Artery Stenosis

NCT07170618 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2025-09-12

No results posted yet for this study

Summary

The primary objective of this trial is to evaluate the safety and efficacy of a new balloon microcatheter in patients with intracranial artery stenosis.

Conditions

  • Intracranial Artery Stenosis

Interventions

DEVICE

balloon microcatheter

The balloon microcatheter simultaneously possesses both balloon dilatation and device delivery functions.

Sponsors & Collaborators

  • Sinomed Neurovita Technology Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2025-09-01
Primary Completion
2025-12-30
Completion
2025-12-30

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 NCT07170618 on ClinicalTrials.gov