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Breast Cancer Registry for Participants With Breast Cancer or Characteristics of Hereditary Breast Cancer

NCT00666731 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4945

Last updated 2023-10-10

No results posted yet for this study

Summary

RATIONALE: Gathering information about patients with breast cancer and their families may help the study of breast cancer in the future.

PURPOSE: This clinical trial is gathering information about patients with breast cancer and their families.

Conditions

Interventions

OTHER

medical chart review

Demographic information (like address and birth date), the results of physical exams, blood tests, x-rays and other diagnostic and medical procedures and treatments, as well as medical and surgical history.

OTHER

questionnaire administration

Collection of personal information, medical history, diet and lifestyle habits, any past or current environmental exposures and to re-create a family tree for any cancers that have occurred in any family members. In accordance with OPRR guidelines, no identifying information such as name, address, or date of birth will be used for relatives, but the affected status (cancer, age of onset, year of birth, age of death) will be recorded.

OTHER

study of socioeconomic and demographic variables

Repository

PROCEDURE

Excess human biological tissue

Tissue procurement.

PROCEDURE

quality-of-life assessment

Cancer care.

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • University of Nebraska

    lead OTHER

Principal Investigators

  • Kenneth H Cowan, MD, PhD · University of Nebraska

Eligibility

Min Age
19 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-10-12
Primary Completion
2016-08-19
Completion
2016-08-19

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00666731 on ClinicalTrials.gov