Transvaginal Ultrasonography as a Screening Method for Ovarian Cancer
-
- STATUS
- Recruiting
-
- participants needed
- 58000
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- sponsor
- John R van Nagell
Summary
This is a large, prospective, single-arm cohort study of transvaginal ultrasonographic
screening for
Description
Women from every Kentucky county participate in the Kentucky
While long-term 20-year survival of women with Type 1
The significance of these findings is that our approach has resulted in the detection of both
early-stage Type 1 and Type 2
The primary objective of this study is to prospectively evaluate the false positive (FP)
percentage generated by the ovarian screening algorithm and determine whether serial
transvaginal
Details
Condition |
Ovarian disorder, |
---|---|
Age | 24years - 100years |
Treatment |
Serial Transvaginal |
Clinical Study Identifier | NCT04473833 |
Sponsor | John R van Nagell |
Last Modified on | 19 February 2024 |
How to participate?
,
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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