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CONVIVO Endomicroscopy

A Feasibility Analysis of an in Vivo CONVIVO Endomicroscopy During Brain Surgery.

Who can join

All ages · All sexes · Healthy volunteers welcome

Inclusion Criteria:

* . The patient is suffering from an intracranial lesion requiring surgery:
* Patients undergoing neurosurgical resection for intrinsic presumably high grade, invasive tumors.
* Patients undergoing neurosurgical resection for other brain tumors,.
* All patient groups will only be comprised of elective surgical patients who have signed the informed consent prior to use

Exclusion Criteria:

* History of hypersensitivity to fluorescein
* History of allergy or bronchial asthma
* Renal failure - Children (patients less than 18 years of age)
* Pregnant women
* Breast feeding women
* Patients with inability to give informed consent

About the study

Visualization of the tissue microstructure during neurosurgery using a non destructive handheld imaging technology producing a real time digital image ("optical biopsy") at cellular resolution is a novel method that holds great promise for optimization and improvement of the surgical treatment of brain pathologies, brain tumors in particular. The goal of this project is to investigate and assess the ease of use of the CONVIVO FDA cleared system in discriminating healthy and abnormal tissues during in vivo use on the brain during neurosurgery in 30 patients with a working diagnosis of intrinsic brain tumors.

What is being tested

• CONVIVO (device)

Sponsor: Northwell Health · Participants: 30 · Started: Jan 8, 2024

Contact the study team

• Betsy Moclair · Phone: 5162537753

Official record on ClinicalTrials.gov — NCT06087393

Locations in the U.S.

Conditions

• Brain Tumors

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.