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Recruiting NCT06087393

NCT06087393 CONVIVO Endomicroscopy

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Clinical Trial Summary
NCT ID NCT06087393
Status Recruiting
Phase —
Sponsor Northwell Health
Condition Brain Tumor
Study Type INTERVENTIONAL
Enrollment 30 participants
Start Date 2024-01-08
Primary Completion 2026-10-12

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type INTERVENTIONAL
Interventions
CONVIVO

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 30 participants in total. It began in 2024-01-08 with a primary completion date of 2026-10-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

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

Contact & Investigator

Central Contact

Betsy Moclair

✉ bmoclair@northwell.edu

📞 5162537753

Frequently Asked Questions

Who can join the NCT06087393 clinical trial?

This trial is open to participants of all sexes, studying Brain Tumor. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06087393 currently recruiting?

Yes, NCT06087393 is actively recruiting participants. Contact the research team at bmoclair@northwell.edu for enrollment information.

Where is the NCT06087393 trial being conducted?

This trial is being conducted at Manhasset, United States.

Who is sponsoring the NCT06087393 clinical trial?

NCT06087393 is sponsored by Northwell Health. The trial plans to enroll 30 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology