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OpenTrials
Completed

NCT Number: NCT00267072

Ovarian Screening Study

The objectives of this study are:

* To identify women at increased risk for developing ovarian cancer * To detect ovarian cancers at an early stage * To investigate the role of tumor membrane fragments as tumor markers for early ovarian carcinoma

Completed

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Key information

About this study

In the year 2001 approximately 23,400 women in the USA are expected to be diagnosed with ovarian carcinoma and 13,900 will die of the disease. This means that within the USA more women die annually from ovarian cancer than all other gynecologic malignancies combined. Within the Commonwealth of Kentucky approximately 250 women per year develop ovarian carcinoma.

Survival for patients with ovarian cancer is directly related to the stage of disease at diagnosis. Unfortunately, the majority of women present with advanced disease (Stage III and IV) and most of these patients will die of the disease.

The aim of screening for ovarian cancer is to reduce the morbidity and mortality by detecting the disease at an early stage since ovarian cancer detected when disease is confined to the ovary (Stage I) is associated with a dramatically improved 5-year survival. Disease confined to the ovary may be cured in over 90% of patients, in some cases without the need for chemotherapy.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Asymptomatic women over the age of 45 with one or both ovaries.
  • Women over the age of 25 with one or both ovaries and any of the following:
  • A personal history of breast, colon or endometrial cancer or breast cancer gene (BRCA) 1 or 2 positive
  • First-degree relative (mother, sister, daughter) with ovarian or breast cancer
  • Two family members with either breast and/or ovarian cancer
  • Mother, sister, daughter, grandparent with a positive BRCA1 or BRCA2 genetic test result.
  • Past use of fertility drugs such as Clomid or Pergonal for more than a year.

Exclusion criteria

  • Women who are symptomatic of ovarian cancer

Sponsors and collaborators

Lead sponsor

University of Louisville

Other

Collaborators

  • James Graham Brown Cancer Center

Registry information

Official study title

The University of Louisville Ovarian Screening Study

Important dates

Study start
2001
Primary completion
2010
Study completion
2010
First posted
Dec 20, 2005
Registry last updated
Jan 9, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.