Evaluation of Tumor Resection Guided by Intraoperative Indocyanine Green Dye Fluorescence Angiography in Patients With Sarcoma
NCT ID: NCT06409013
Last Updated: 2025-09-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
50 participants
OBSERVATIONAL
2024-03-14
2027-03-30
Brief Summary
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Detailed Description
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I. To evaluate the use of indocyanine green (ICG) as an intraoperative guide during bone and soft tissue sarcoma resection.
OUTLINE: This is an observational study.
Patients receive ICG infusion prior to undergoing scheduled resection and have medical records reviewed on study.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Observational
Patients receive ICG infusion prior to undergoing scheduled resection and have medical records reviewed on study.
Non-Interventional Study
Non-interventional study
Interventions
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Non-Interventional Study
Non-interventional study
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Chronic kidney disease
* Anaphylaxis to dyes
18 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Principal Investigators
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Matthew T. Houdek, M.D.
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic in Rochester
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Central Contacts
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Facility Contacts
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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NCI-2024-03482
Identifier Type: REGISTRY
Identifier Source: secondary_id
23-003589
Identifier Type: OTHER
Identifier Source: secondary_id
23-003589
Identifier Type: -
Identifier Source: org_study_id
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