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Clinical Trials (PDQ®)
Patient Version   Health Professional Version
Last Modified: 5/14/2008     First Published: 6/1/2002  
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Clinical Trial to Screen Participants Who Are at High Genetic Risk for Ovarian Cancer

Alternate Title
Basic Trial Information
Trial Description
     Purpose
     Eligibility
     Treatment/Intervention
Trial Contact Information
Registry Information

Alternate Title

Pilot Screening Study for Ovarian Cancer in Participants Who are at High Genetic Risk for Developing Ovarian Cancer

Basic Trial Information

Phase
Type
Status
Age
Sponsor
Protocol IDs

No phase specified


Screening


Active


30 and over


NCI


MGH-000084
NCT00039559

Trial Description

Purpose:

Screening tests may help doctors detect cancer cells early and plan more effective treatment for ovarian cancer.

Screening trial to determine the significance of CA 125 levels in detecting ovarian cancer in participants who have a high genetic risk of developing ovarian cancer.

Eligibility:

Eligibility criteria include the following:

Final eligibility for a clinical trial is determined by the health professionals conducting the trial.

Treatment/Intervention:

Blood samples will be collected and patients will complete questionnaires every 3 months for up to 7 years. Some patients may also undergo transvaginal ultrasound. Patients will be evaluated periodically for 1 year after completing the study.

Important:

For more details about this trial, refer to the Health Professional version of the trial summary.

If you are interested in participating in a clinical trial, contact your doctor for a referral or call a trial contact person listed below. You may see the same contact person listed at more than one site, however, if you call the number listed you can ask to speak to the study coordinator or person involved with the specific trial you are interested in. If you have questions about cancer or clinical trials, call the Cancer Information Service at 1-800-4-CANCER (1-800-422-6237). General information about clinical trials, including risks, benefits, and costs, can be found on NCI's Web site.

Trial Contact Information

Trial Lead Organizations

Massachusetts General Hospital

Steven J. Skates, PhD, Protocol chair
Ph: 617-724-9913; 877-726-5130

Trial Sites

U.S.A.
California
  Orange
 Chao Family Comprehensive Cancer Center at University of California Irvine Medical Center
 Clinical Trials Office - Chao Family Comprehensive Cancer Center
Ph: 877-UC-STUDY
 Email: ucstudy@uci.edu
Connecticut
  New Haven
 Yale Cancer Center
 Clinical Trials Office - Yale Cancer Center
Ph: 203-785-5702
Iowa
  Des Moines
 John Stoddard Cancer Center at Iowa Methodist Medical Center
 Clinical Trials Office - John Stoddard Cancer Center at Iowa Methodist Medical Center
Ph: 515-241-6727
Massachusetts
  Boston
 Massachusetts General Hospital
 Clinical Trials Office - Massachusetts General Hospital
Ph: 877-726-5130
Nebraska
  Omaha
 Creighton University Medical Center
 Clinical Trials Office - Creighton University Medical Center
Ph: 402-280-4100
North Carolina
  Chapel Hill
 Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
 Clinical Trials Office - Lineberger Comprehensive Cancer Center
Ph: 877-668-0683; 919-966-4432
  Durham
 Duke Comprehensive Cancer Center
 Clinical Trials Office - Duke Comprehensive Cancer Center
Ph: 888-275-3853
Texas
  Houston
 M. D. Anderson Cancer Center at University of Texas
 Clinical Trials Office - M. D. Anderson Cancer Center at the University of Texas
Ph: 713-792-3245
  San Antonio
 University of Texas Health Science Center at San Antonio
 Maria Romero
Ph: 210-562-1586

Registry Information
Official Title Ovarian Cancer Screening Pilot Trial in High Risk Women
Trial Start Date 2002-05-14
Registered in ClinicalTrials.gov NCT00039559
Date Submitted to PDQ 2002-04-17
Information Last Verified 2008-04-04

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