Investigating the Use of Fluorescence Imaging in Endometrial Cancer Surgery
Completed · Not applicable
Conditions studied: Endometrial Cancer
In brief
The main purpose of the study is to evaluate the detection rate and accuracy of fluorescence imaging in endometrial cancer staging by sentinel node assessment.
Key facts
- Study ID
- NCT01562106
- Run by
- Swedish Medical Center
- People needed
- 123
- Starts
- 2012-02-01
- Expected to finish
- 2016-08-01
- Last updated by the study team
- 2016-11-18
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Biopsy proven endometrial carcinoma
- Must have planned to undergo standard endometrial cancer staging surgery as part of their routine clinical care
- Must be 18 years of age and older
- Must be able to comply with all the study procedures
You may not qualify if…
- Significant liver disease, cirrhosis or liver insufficiency with abnormal liver function tests, with total bilirubin > 1.5 times normal, and/or SGOT > 2 times normal
- Uremia, serum creatinine > 2.0 mg/dl
- Previous history of adverse reaction or allergy to ICG dye, iodine, shellfish, or iodine dyes
- Previous lymphadenectomy or surgery that could change the uterine lymphatic drainage
- Pregnant
- Currently participating in a drug, biologic and/or device treatment study
- Any medical condition that would normally prevent someone from receiving general anesthesia or undergoing standard surgical procedures
Where it is running
- Swedish Medical Center Issaquah Campus — Issaquah, Washington, United States
- Pacific Gynecology Specialists — Seattle, Washington, United States
- Swedish Medical Center — Seattle, Washington, United States
Full record on ClinicalTrials.gov
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