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Feasibility of Performing Peripheral Pulmonary Lesion Biopsy Using Robotic Bronchoscopy-Guided Cryoprobe

NCT05399082 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-10-17

Study results available
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Summary

This research is being done to evaluate the feasibility, and biopsy quality, of using a 1.1mm disposable cryoprobe that is passed through the working channel of the Ion Robotic bronchoscope to collect biopsy tissue.

Conditions

  • Bronchi--Diseases
  • Lung Diseases, Obstructive
  • Lesions Mass

Interventions

DEVICE

Cryoprobe biopsy

A 1.1mm disposable cryoprobe that is passed through the working channel of the Ion Robotic bronchoscope to collect biopsy tissue

PROCEDURE

Forceps biopsy

Biopsy forceps used to collect tissue

Sponsors & Collaborators

  • Erbe USA Incorporated

    collaborator OTHER

  • Mayo Clinic

    lead OTHER

Principal Investigators

  • Ryan Kern, MD · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-15
Primary Completion
2023-07-11
Completion
2023-07-11
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT05399082 on ClinicalTrials.gov