A Study of Intra-operative Imaging in Women With Ovarian Cancer
Recruiting now · Phase 3
Conditions studied: Ovarian Cancer, Ovarian Carcinoma
In brief
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.
Key facts
- Study ID
- NCT04878094
- Run by
- Memorial Sloan Kettering Cancer Center
- People needed
- 310
- Starts
- 2021-05-03
- Expected to finish
- 2027-05-03
- Last updated by the study team
- 2026-05-20
Who can join
Age: any. Sex: female. Healthy volunteers: not accepted.
Where it is running
- Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities) — Basking Ridge, New Jersey, United States (enrolling)
- Memorial Sloan Kettering Monmouth (Limited Protocol Activities) — Middletown, New Jersey, United States (enrolling)
- Memorial Sloan Kettering Bergen (Limited Protocol Activities) — Montvale, New Jersey, United States (enrolling)
- Memorial Sloan Kettering Cancer Center @ Suffolk - Commack (Limited Protocol Activities) — Commack, New York, United States (enrolling)
- Memorial Sloan Kettering Westchester (Limited Protocol Activities) — Harrison, New York, United States (enrolling)
- Memorial Sloan Kettering Cancer Center (All Protocol Activities) — New York, New York, United States (enrolling)
- Memorial Sloan Kettering Nassau (Limited Protocol Activities) — Uniondale, New York, United States (enrolling)
- Jefferson Abington Hospital — Willow Grove, Pennsylvania, United States (enrolling)
- Houston Methodist Cancer Center (Data Collection Only) — Houston, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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