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Clinical Trials/NCT05305378
NCT05305378
Completed
Not Applicable

Intraoperative Laser Speckle Contrast Imaging of Cerebral Blood Flow

Dynamic Light1 site in 1 country8 target enrollmentApril 20, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aneurysm, AVM, Dural Arteriovenous Fistula, Glioma, Meningioma, Metastasis, Bypass
Sponsor
Dynamic Light
Enrollment
8
Locations
1
Primary Endpoint
Agreement of ICG and LSCI.
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of the proposed study is to investigate the usefulness of laser speckle contrast imaging (LSCI) compared to indocyanine green angiography (ICGA). We will collect data from a wide variety of neurovascular surgical procedures to determine when the technology is the most clinically useful. The intraoperative LSCI system provides high resolution images of blood flow in real-time without tissue contact and without the need for an exogenous contrast agent. Further study is needed to gain a better understanding of the use of the technique during surgery, but initial results suggest that the ability to identify blood flow changes with immediate feedback to the surgeon could be a significant advantage during many procedures.

Detailed Description

Cerebral blood flow (CBF) is of paramount importance to human brain function, as the brain relies on a continuous blood supply to meet its energy needs. Blockage of a cerebral blood vessel during the course of surgery, even if transient and short-lived, may result in irreversible brain tissue damage (i.e. stroke) and loss of cortical function, if not identified quickly enough. During neurosurgery, vessel occlusion may occur either inadvertently or as a necessary part of the procedure, and yet current technologies do not adequately predict the consequences of such occlusion. Real-time CBF visualization during surgery could help neurosurgeons better understand the consequences of vascular occlusion events during surgery, recognize potential adverse complications, and thus prompt timely intervention to reduce the risk of stroke. The current standard for visualizing CBF during surgery is indocyanine green angiography (ICGA), which involves administering a bolus of fluorescent dye intravenously and imaging the wash-in of the dye to determine which vessels are perfused. Unfortunately, ICGA can only be used a few times during a surgery due to the need to inject a fluorescent dye, and provides only an instantaneous view of perfusion rather than a continuous view. Patients will undergo standard craniotomy surgery. The surgical procedures will not be altered in any way by the proposed studies. As long as it is standard of care, neuromonitoring, intraoperative angiogram, and Indocyanine green angiography will be performed by the surgeon. LSCI imaging will be performed at the discretion of the surgeon following exposure of the cortex and will vary from patient to patient depending on the neurosurgical procedure. The LSCI measurements will not add any time to the surgery nor affect the normal operation of the neurosurgical microscope.

Registry
clinicaltrials.gov
Start Date
April 20, 2022
End Date
August 31, 2022
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Dynamic Light
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adults (18 years or older).
  • Size of craniotomy at least 2 cm.
  • Possibility of intraoperative ICGA.
  • Able to render written informed consent.
  • Women of child-bearing potential must have a negative pre-op pregnancy test.

Exclusion Criteria

  • Patients unable to legally consent.
  • Patients with impaired cognitive function.

Outcomes

Primary Outcomes

Agreement of ICG and LSCI.

Time Frame: During Surgery

Agreement of ICG and LSCI observations to determine flow in exposed vessels classified as no flow, delayed flow, or normal flow.

Study Sites (1)

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