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Clinical Trial Summary

This is a prospective observational study that will evaluate the association between bone and tissue perfusion, as measured by indocyanine green (ICG) fluorescence imaging, and complications, in an effort to develop ICG fluorescence imaging as a diagnostic tool to quantitatively guide operative debridement.


Clinical Trial Description

This is a prospective observational study that will evaluate the association between bone and tissue perfusion, as measured using indocyanine green (ICG) fluorescence imaging, and complications. This will be used to develop ICG fluorescence imaging as a diagnostic tool to objectively and quantitatively guide operative debridement. The study population includes all open fracture patients regardless of race, ethnicity, or sex/gender. Primary outcome measure is all-cause re-operation and secondary outcome measure is surgical site infection. All patients will be followed for a total of 12 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04416412
Study type Observational [Patient Registry]
Source Dartmouth-Hitchcock Medical Center
Contact Jon Mikael Anderson
Phone 603-653-3306
Email jon.mikael.anderson@hitchcock.org
Status Recruiting
Phase
Start date October 1, 2020
Completion date January 31, 2026

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