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Clinical Trials/NCT00531778
NCT00531778
Terminated
Not Applicable

NYU Ovarian Cancer Early Detection Program Blood and Genetics

NYU Langone Health1 site in 1 country890 target enrollmentJune 2004
ConditionsOvarian Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ovarian Cancer
Sponsor
NYU Langone Health
Enrollment
890
Locations
1
Primary Endpoint
identification and development of highly sensitive and specific tumor markers for ovarian cancer
Status
Terminated
Last Updated
15 years ago

Overview

Brief Summary

Improving current strategies for detection of early stage disease can impact favorably on long-term survival of women with ovarian cancer. To reduce the morbidity and mortality of ovarian cancer, screening for this disease must detect early stage disease rather than advanced stage disease. Thus the challenge for the future is to identify and develop highly sensitive and specific tumor markers that can be applied to population-based screening for the early detection of ovarian cancer.

Detailed Description

The aim of NYU Ovarian Cancer Early Detection Program is to establish an effective, early detection program employing state-of-the-art science and technology in collaboration with other nationally recognized clinicians and scientists. This proposed research study will foster collaboration between clinicians and scientists that will facilitate the rapid identification of a set of molecular, biochemical, functional, and genetic markers which can be employed to effectively detect and manage ovarian cancer and other gynecological malignancies.

Registry
clinicaltrials.gov
Start Date
June 2004
End Date
November 2010
Last Updated
15 years ago
Study Type
Observational
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • Women enrolled in the NYU Ovarian Cancer Early Detection Program have at least one of the following risk factors:
  • A personal history of breast cancer
  • One or more first degree relatives (mother, sister, daughter) with ovarian cancer
  • Multiple family members with either breast and/or ovarian cancer
  • A personal history of a positive BRCA1 or BRCA2 genetic test result
  • A close relative with a positive BRCA1 or BRCA2 genetic test result
  • A personal history of colon or endometrial cancer with at least two relatives with a Lynch/HNPCC-associated cancer (colorectal, endometrial, small bowel, ureter, or renal pelvis cancer)
  • Synchronous or metachronous endometrial and colorectal cancer
  • A personal history of a mismatch repair gene mutation (MLH1, MSH2, MSH6 or PMS2)
  • A close relative with a mismatch repair gene mutation (MLH1, MSH2, MSH6 or PMS2)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

identification and development of highly sensitive and specific tumor markers for ovarian cancer

Time Frame: 5 years

Study Sites (1)

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