An interventional study of Continuous glucose monitoring system in Reconstructive Tissue Surgery, sponsored by University of Wisconsin, Madison. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-03-20.
Sponsored by University of Wisconsin, Madison · Not applicable, Interventional, and Diagnostic
The purpose of this study is to determine if 1) a continuous glucose monitoring system can measure glucose levels in transferred tissue during reconstructive surgery, and 2) if glucose measurements from a continuous glucose monitoring system correlate with tissue blood perfusion.
University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.
Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Subjects have sensors placed on skin before surgery and these sensors will measure the subject's glucose until the third day after surgery when they are removed.
Device: Continuous glucose monitoring system
one or two monitors will be placed in the tissue to be transferred
Perfusion and tissue transfer outcome during reconstructive surgery predicted by continuous glucose monitoring of tissue
Time frame: Up to three days post-op
This study is withdrawn, as verified in Mar 2018. You cannot join it, but the record below documents what was studied.
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University of Wisconsin, Madison