Recruiting

ORBEYE

Sponsor:

Northwell Health

Code:

NCT04937244

Conditions

Malignant Glioma of Brain

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

5ALA exoscopic fluorescence filter

Study Details

Brief summary:

Fluorescence-guided resection using 5-ALA induced tumor fluorescence of malignant gliomas allows for better identification of tumor tissue and more radical resection in select patients and improvements in progression-free and overall survival. With new developments in surgical microscopy, the development of digital exoscopes have provided advanced visualization as well as improvements in ergonomics and accessibility of the surgical field. The use of the exoscope in 5-ALA fluorescence-guided tumor surgery has the potential to enhance the ability of the surgeon to remove brain tumors with high efficacy. While algorithms for use of 5-ALA fluorescence have been optimized for use with traditional microscopes, the use of fluorescence techniques in newer digital exoscopes have not been developed. The primary outcome of the study is to obtain parameters to optimize visualization of fluorescence intensity and perform optimization based on the intensities achieved. The operating ORBEYE exoscope will be fitted with a blue light filter. All experiments will be performed in darkened operating rooms. The ORBEYE exoscope will be set up at constant distances from the target and incident light intensities. The focal distance and light intensity settings will be recorded from the data displayed on the microscope. Patients (experimental group) will receive 5ALA treatment before operation, blue light filter imagining will take place after tacking up dura and prior to direct resection. The expected outcomes of image analysis will be to have a set of exoscope parameters optimized for visualization of 5ALA tissue in different tumor types. This 5ALA characterization of visualization parameters has never been completed on an exoscope. Optimizing ORBEYE exoscope parameters will define a standard in glioma resection using 5ALA under a novel exoscopic filter as well as contribute insight into the use of the fluorescent filter for additional tumor types.

Conditions

Malignant Glioma of Brain

Study ID

NCT04937244

Start date

May 13, 2021

Status verified date

Jun, 2021

Completion date

May 11, 2022

Anticipated

Primary completion date

May 11, 2022

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Male and female ≥ 18 years of age
  • Must have a suspected or biopsy-proven glioma (World Health Organization grade II or IV), new or recurrent
  • Indication for craniotomy for removal of a suspected or recurrent brain tumor
  • Karnofsky Performance Scale ≥ 60%
  • Willing and able to provide informed consent or have surrogate consent by legally authorized representative

Exclusion Criteria:

  • Male and female < 18 years of age
  • Porphyria, hypersensitivity to porphyrins
  • Renal insufficiency as defined by a creatinine > 2.0 mg/dL
  • Hepatic insufficiency as diagnosed in preoperative medical clearance evaluation
  • Females of childbearing potential with a positive pregnancy test
  • Nursing women
  • Unwilling or unable to provide informed consent

Study Design

Enrollment

10 participants

Anticipated

Intervention Model

Single group

Primary purpose

Device Feasibility

Interventions and Outcome Measures

Arms

experimental: Patients with new or recurrent malignant gliomas

Interventions

5ALA exoscopic fluorescence filter

Visualization of tumor tissue with 5ALA will be done in the operating room to localize neoplastic tissue. The operation will be conducted in a standard fashion uninfluenced by the imaging on the ORBEYE exoscope. The ORBEYE exoscope will be used with the blue light filter after tacking up dura upon first visualization of tumor tissue prior to direct resection. Images will be taken prior to, during and at the end of the planned resection. The ORBEYE exoscope will be set up at constant distances from the target and incident light intensities. The focal distance and light intensity settings will be recorded from the data displayed on the microscope. The ORBEYE exoscope or standard operating microscope (depending on surgeon preference) will then be used in the standard fashion of an operative microscope with a fluorescent filter, to assist with surgical resection as per the surgeon's preference. Resection will proceed according to current standard of care.

Primary outcome measure

  • Focal Distance [ Time Frame: 6 weeks ]
  • Light Intensity [ Time Frame: 6 weeks ]
  • Working Angle [ Time Frame: 6 weeks ]

Central Contacts and Locations

Locations

Lenox Hill Hospital

Recruiting

New York, New York, United States, 10075

Contacts

Principal Investigator:

Randy D'Amico, MD

More Information

Sponsor

Northwell Health

Last update posted

Jun 23, 2021

Last verified

Jun, 2021

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Northwell Health on 2021-06-23.