Ovarian Screening Study

NCT ID: NCT00267072

Last Updated: 2018-01-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

5000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2001-06-30

Study Completion Date

2010-05-31

Brief Summary

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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

Detailed Description

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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.

Conditions

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Ovarian Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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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
Minimum Eligible Age

25 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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James Graham Brown Cancer Center

OTHER

Sponsor Role collaborator

University of Louisville

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Cyril W. Helm, MD

Role: PRINCIPAL_INVESTIGATOR

University of Louisville, James Graham Brown Cancer Center

Locations

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James Graham Brown Cancer Center

Louisville, Kentucky, United States

Site Status

Countries

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United States

References

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Greenlee RT, Hill-Harmon MB, Murray T, Thun M. Cancer statistics, 2001. CA Cancer J Clin. 2001 Jan-Feb;51(1):15-36. doi: 10.3322/canjclin.51.1.15.

Reference Type BACKGROUND
PMID: 11577478 (View on PubMed)

Other Identifiers

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328.01

Identifier Type: -

Identifier Source: org_study_id

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