CompletedNot Applicable

Needle-based Confocal Laser Endomicroscopy in Fluoroscopy-guided Procedures

France6 participantsStarted 2015-01

Plain-language summary

This study is a prospective study in order to demonstrate the technical feasibility and safety of doing endomicroscopic imaging during interventional radiology procedure in two main indications: lung and liver. This innovative study will involve the use of probe-based confocal laser endomicroscopy. The proposed study is a feasibility study.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients scheduled to have an interventional radiology procedure for needle-biopsy or radiofrequency ablation purposes in lung or in liver, 18 years or older. * Only subjects who have provided written informed consent for the study can be included in the study. Exclusion Criteria: * Known allergy to fluorescein * Previous life-threatening allergic reactions and known hypersensitivity to contrast media * Pregnancy or breast-feeding * History of cardio-pulmonary disease (including bronchial asthma) * Restricted renal function * Elderly with diabetes mellitus * Patients under a beta-blockers treatment

What they're measuring

Measure adverse events frequency in the use of mini probes on the tumor

Timeframe: Up to 1 week

Trial details

NCT IDNCT02224885

SponsorMauna Kea Technologies

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2016-03

View on ClinicalTrials.gov More Lung Percutaneous Biopsy trials