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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04351373
Other study ID # 19-005178
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date October 6, 2021
Est. completion date May 25, 2022

Study information

Verified date July 2023
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if there is benefit to using an IV contrast called AK-Fluor® and a microscope filter called YELLOW560 when surgically removing a vestibular schwannoma, Meningioma, Head and Neck Paraganglioma, or Head and Neck Schwannoma.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date May 25, 2022
Est. primary completion date May 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria - Patient with a suspected VS - Recurrent VS with prior microsurgical resection or radiation therapy - Clinical indication for microsurgical resection Exclusion Criteria - History of allergy to FS - History of renal failure - Pregnant women - Those with inability to give informed consent - Prisoners and inmates

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Fluorescein Sodium
Intravenous administration 1 mg/kg initial dosing if insufficient additional doses of 1 mg/kg may be administered.
Device:
YELLOW560 filter
Integrated fluorescence module serves to make fluorescent areas visible to assist in visualizing tumor during the resection.

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

References & Publications (1)

Chan SA, Macielak RJ, Tuchscherer AM, Neff BA, Driscoll CLW, Peris-Celda M, Van Gompel JJ, Link MJ, Carlson ML. Fluorescein-Assisted Microsurgical Resection of Vestibular Schwannoma: A Prospective Feasibility Study. Otol Neurotol. 2022 Dec 1;43(10):1240-1 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Surgeon Predicted Use of Fluorescein Sodium in Future Cases Physician response to surgeon survey question, "Based on the use and performance of FS in this case alone, how likely are you to use FS in future cases (excluding the research trial) involving this tumor?" using a Likert-style rating from 0-4 where 0=Unsure; 1= Plan to not use in any cases; 2= Plan to use in select cases; 3=Plan to use in the majority of cases; 4=Plan to use in all cases. Approximately 3 months postoperatively
Primary Correlation of Fluorescein Sodium With Surgeons' Visual Assessment Fluorescence correlate with surgeons' visual assessment of the tumor and nerve tissue under normal microscopy without the Yellow 560 filter using a Likert-style rating from 1-4 where 1=No correlation; 2=Some correlation; 3=Good correlation; 4=Excellent correlation. Intraoperatively, approximately 1 day
Primary Correlation of Fluorescein Sodium With Electrostimulation Surgeons' assessment of fluorescence correlate with electrostimulation (e.g. tissues with high fluorescence do not stimulate, whereas nerve tissues with low fluorescence do stimulate)" using a Likert-style rating from 1-4 where 1=No correlation; 2=Some correlation; 3=Good correlation; 4=Excellent correlation. Intraoperatively, approximately 1 day
Secondary Time to Differential Visualization The amount of time in minutes for differential visualization of the tumor and surrounding tissue after sodium fluorescein administration during surgery Intraoperatively, approximately 1 day
Secondary Average Dose of Sodium Fluorescein Administration Average dose of sodium fluorescein administered during surgery to achieve differential fluorescence of the tumor and tissue reported in mg/kg Intraoperatively, approximately 1 day
Secondary Total Resection Rate Number of subjects to have a gross total resection Intraoperatively, approximately 1 day
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