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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00666731
Date of registration: 24/04/2008
Primary sponsor: University of Nebraska
Public title: A Breast Cancer Information Registry for Participants With Breast Cancer or Characteristics of Hereditary Breast Cancer BCCR
Scientific title: Development and Implementation of The Breast Cancer Collaborative Registry (BCCR)
Date of first enrolment: October 2006
Target sample size: 999999
Recruitment status: Recruiting
URL:  http://clinicaltrials.gov/show/NCT00666731
Study type:  Observational
Study design:  Time Perspective: Prospective  
Countries of recruitment
United States
Contacts
Name:   Elizabeth "Liz" Fleissner, RN BSN
Address: 
Telephone: 402-559-8197
Email: eafleissner@unmc.edu
Affiliation: 
Name:   Kenneth H. Cowan, MD, PhD
Address: 
Telephone:
Email:
Affiliation:  University of Nebraska
Key inclusion & exclusion criteria

DISEASE CHARACTERISTICS:

- Recruited by a participating physician and meets at least 1 of the following
criteria:

- Current diagnosis or history of breast cancer, atypical hyperplasia, ductal
carcinoma in situ (DCIS) or lobular carcinoma in situ (LCIS) as defined in the
National Comprehensive Cancer Network Breast and/or Ovarian Genetic Assessment
Guidelines, v.1.2006

- Characteristics of hereditary breast cancer, as defined in the National
Comprehensive Cancer Network Breast and/or Ovarian Genetic Assessment
Guidelines, v.1.2006 (relatives have been diagnosed with breast and/or ovarian
cancer) OR have a breast cancer risk of > 1.67% over 5 years as estimated by the
GAIL Model

- Hormone receptor status not specified

PATIENT CHARACTERISTICS:

- Male or female

- Menopausal status not specified

PRIOR CONCURRENT THERAPY:

- Not specified



Age minimum: 19 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Breast Cancer
Precancerous Condition
Intervention(s)
Other: medical chart review
Other: questionnaire administration
Other: study of socioeconomic and demographic variables
Procedure: Excess human biological tissue
Procedure: quality-of-life assessment
Primary Outcome(s)
Implementation of a web-based Breast Cancer Collaborative Registry at the National Comprehensive Cancer Network (NCCN) centers [Time Frame: Ongoing]
Merger of data collected under the Adult Oncology Data Collection Study and the National Comprehensive Cancer Network Data Coordinating study at UNMC/NMC [Time Frame: Ongoing]
Standardization of clinical, environmental, socio-demographic, and family history data collected for breast cancer-related research and shared by the Eppley Breast Cancer Research Group collaborators [Time Frame: Ongoing]
Secondary Outcome(s)
Secondary ID(s)
311-06
P30CA036727
UNMC-31106
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
National Cancer Institute (NCI)
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