RECRUITING

CONVIVO Endomicroscopy

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-01-08
Study Completion:2024-10-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06087393

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * . The patient is suffering from an intracranial lesion requiring surgery:
  2. * Patients undergoing neurosurgical resection for intrinsic presumably high grade, invasive tumors.
  3. * Patients undergoing neurosurgical resection for other brain tumors,.
  4. * All patient groups will only be comprised of elective surgical patients who have signed the informed consent prior to use
  1. * History of hypersensitivity to fluorescein
  2. * History of allergy or bronchial asthma
  3. * Renal failure - Children (patients less than 18 years of age)
  4. * Pregnant women
  5. * Breast feeding women
  6. * Patients with inability to give informed consent

Contacts and Locations

Study Contact

Betsy Moclair
CONTACT
5162537753
bmoclair@northwell.edu

Study Locations (Sites)

Northwell Health
Manhasset, New York, 11030
United States

Collaborators and Investigators

Sponsor: Northwell Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-01-08
Study Completion Date2024-10-12

Study Record Updates

Study Start Date2024-01-08
Study Completion Date2024-10-12

Terms related to this study

Additional Relevant MeSH Terms

  • Brain Tumor