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Clinical Study of Coronary Extension Catheter

NCT07742345 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2026-08-03

No results posted yet for this study

Summary

This prospective, multicenter, single-arm study plans to enroll 69 subjects. Subjects meeting the protocol criteria will receive treatment with coronary extension catheters. The safety and efficacy of these catheters in percutaneous coronary intervention will be assessed through the collection and analysis of efficacy and safety endpoints during treatment and follow-up.

Conditions

  • Coronary Artery Disease (CAD)
  • Percutaneous Coronary Intervention (PCI)

Interventions

DEVICE

Coronary Extension Catheter

For the subjects who met the requirements of the study protocol, the BM coronary extension catheter was used for treatment.

Sponsors & Collaborators

  • BrosMed Medical Co., Ltd

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-25
Primary Completion
2027-04-30
Completion
2027-04-30

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 NCT07742345 on ClinicalTrials.gov