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Clinical Trials in Canada / NCT05948904
Recruiting Not applicable

Defining a Technique for the Use of Cryogenic Catheters for Biopsy and Ablation for the Diagnostic and Treatment of Pulmonary Lesions: An Ex-Vivo Human Lung Model Study.

NCT05948904 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2023-11-03
Last updated
2026-03-18

Condition(s) studied

Lung Diseases

Investigational drug(s) / intervention(s)

Cryo Ex Vivo

Cryo Ex Vivo: Lungs from patients undergoing lung transplantation after their removal from the recipient patient with previous informed consent signed before transplantation will be obtained. The organs will be placed in an acrylic box and will be kept at a temperature of 37 Celsius degrees. The lungs will be mechanically ventilated connected by an endotracheal tube size 8 inserted in the bronchus with the balloon inflated and a silk suture providing a hermetic closure proximal to the balloon. Tissue samples will be taken from the models and images will be performed.

Study summary

Developing a standardized methodology for the use of novel cryogenic catheters for transbronchial cryobiopsy and cryoablation of pulmonary lesions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients undergoing lung transplant surgery Exclusion Criteria: * Organ donor ineligible to donate lungs * Healthy individuals

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHUM Montreal Quebec Recruiting

More Centre hospitalier de l'Université de Montréal (CHUM) trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05948904 on ClinicalTrials.gov ↗ ← All trials in Canada