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Brief Title: Compare Fallopian Tube Cells Collected by Cytuity With Removed Ovarian/Tubal Tissue to Determine Presence of Malignancy
Official Title: The nCYT Study: A Powered Study to Evaluate the Sensitivity and Specificity of Cytological Evaluation of Fallopian Tube Samples Collected by the Cytuity in Determining the Presence of Malignancy
Study ID: NCT03593681
Brief Summary: Prospective, multi-center, non-randomized study to assess the ability of the Cytuity device to collect cell samples from the fallopian tube that can be evaluated for the presence or absence of malignancy.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Scripps Clinic Medical Group, San Diego, California, United States
Kaiser Permanente San Francisco Medical Center, San Francisco, California, United States
Mayo Clinic, Jacksonville, Florida, United States
Mayo Clinic, Rochester, Minnesota, United States
New York Presbyterian Hospital, New York, New York, United States
Pennsylvania Hospital, Philadelphia, Pennsylvania, United States
Vanderbilt University Medical Center, Nashville, Tennessee, United States
Baylor Scott & White Research Institute, Fort Worth, Texas, United States
University of Virginia, Charlottesville, Virginia, United States
Swedish Health Services, Seattle, Washington, United States
Name: Ted L Anderson, MD,PhD,FACOG
Affiliation: Vanderbilt University Medical Center
Role: PRINCIPAL_INVESTIGATOR