Clinical trial · Observational
NYU Ovarian Cancer Early Detection Program Blood and Genetics
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): insufficient funding and resource
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Ovarian Cancer | Malignant Ovarian Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (0)
Data not yet available
Design
Arms and outcomes
Arms (1)
- label
- NYU OCEDP Population
Primary outcomes (1)
- measure
- identification and development of highly sensitive and specific tumor markers for ovarian cancer
- timeFrame
- 5 years
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
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) * A personal history of colorectal or endometrial cancer with a mismatch repair defect (ie. Microsatellite instability (MSI) or immunohistochemical loss of expression of MLH1, MSH2, MSH6, or PMS2) * The use of fertility drugs for more than one year
References
Publications (0)
Data not yet available