MedTrace Logo

Airway Bypass - Safety and Feasibility Study

NCT06249529 · Status: RECRUITING · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2024-02-08

No results posted yet for this study

Summary

The objective of this study is to evaluate its safety and feasibility of the Airway Bypass Stent System in patients with severe emphysema. The study will collect clinical data through 12 months to assess procedural and device safety.

Conditions

  • Emphysema or COPD

Interventions

DEVICE

Airway Bypass

Bypass stent(s) are implanted to allow air trapped in the parenchyma to escape

Sponsors & Collaborators

  • Zoar Engelman

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2024-01-26
Primary Completion
2025-06-01
Completion
2026-06-01

Countries

  • Georgia

Study Locations

More Related Trials

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 NCT06249529 on ClinicalTrials.gov