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Clinical Trial Summary

The purpose of this study is to find out whether using the PINPOINT imaging system intra-operatively can reduce the risk of anastomotic leaks and other complications after surgery for ovarian cancer, compared with standard intra-operative assessments alone. The PINPOINT endoscopic fluorescence imaging system uses a special camera and a fluorescent (glowing) dye that can evaluate the blood flow of the bowel in real-time. If there is an area that appears concerning, the surgeon can correct the problem during the procedure.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04878094
Study type Interventional
Source Memorial Sloan Kettering Cancer Center
Contact Mario Leitao, MD
Phone 212-639-3987
Email leitaom@mskcc.org
Status Recruiting
Phase Phase 3
Start date May 3, 2021
Completion date May 3, 2025

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