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Clinical Trial Summary

A study for dosage-image optimization of 6% hydroxyethyl starch diluted indocyanine green for near-infrared fluorescence navigated sentinel lymph node mapping for breast cancer patient.


Clinical Trial Description

Pre-clinical experiment has shown using 6% hydroxyethyl starch (Voluven®) as a solvent, compared with pure water, can improve brightness of indocyanine green particles at the same concentration. Similar findings have been addressed using human serum albumin as a solvent for indocyanine green in previous studies, but there was no report using 6% hydroxyethyl starch as a solvent till now. This study aims for clinical translation and optimization of 6% hydroxyethyl starch diluted indocyanine green in breast cancer patients undergoing sentinel lymph node biopsy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05365204
Study type Interventional
Source National Taiwan University Hospital Hsin-Chu Branch
Contact Yung-Chun Hsieh, MD
Phone +886-972322925
Email [email protected]
Status Recruiting
Phase Phase 1
Start date April 8, 2022
Completion date April 7, 2023

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