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OpenTrials
Completed

NCT Number: NCT00943241

Screening in Myocardial Perfusion Patients

To expand the understanding of the uptake and distribution of Tc-99m sestamibi in the breast in a normal female population undergoing myocardial perfusion imaging using Molecular Breast Imaging (MBI).

Completed

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Key information

Age range

18 year–90 year

Sex eligibility

Female

Study type

Observational

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

About this study

You are being asked to take part in this research study because you have been scheduled to have a scan of your heart. The radioactive dye used to image your heart is also taken up by many types of breast cancer. The investigators have developed a new method for detecting breast cancer, called Molecular Breast Imaging that uses this dye.

The purpose of this study is to see how well this new method works in normal subjects with no known breast cancer and to see if we can detect breast cancer at an earlier stage than mammography. As you read this form describing the study, ask any questions you have. Take your time to decide. Feel free to discuss the study with your family, friends, and healthcare provider before you decide. You may stop participating at any time during the study. You may decide not to participate. If so, none of your current benefits or normal health care will be affected in any way. When you feel comfortable that all your questions have been answered, and you wish to take part in this study, sign this form in order to begin your participation. Your signature means you have been told about the study and what the risks are. Your signature on this form also means that you want to take part in this study.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • They have had a mammogram at Mayo Clinic Rochester within the last 12 months
  • Undergoing myocardial perfusion imaging

Exclusion criteria

  • They are unable to understand and sign the consent form
  • They are physically unable to sit upright and still for 20 minutes
  • They have undergone breast surgery or breast biopsy within the last 12 months.
  • They have had trauma to the breast tissue or undergone radiation treatment to the breast within the last 12 months.

Treatment and study plan

Primary outcomes

  1. Biopsy-proven breast cancer

    Time frame: 12 months

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Collaborators

  • Gamma Medica-Ideas

Registry information

Official study title

Screening for Breast Cancer in Patients Undergoing Myocardial Perfusion Imaging

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
Jul 22, 2009
Registry last updated
Feb 13, 2013

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.

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