Houston, Texas 77030


Purpose:

Any time the words "you," "your," "I," or "me" appear, it is meant to apply to the potential participant. The goal of this laboratory research study is to collect and store blood and tissue from patients who have a diagnosis of heart disease and may be at a high risk for the development of heart failure. This blood may be used in the future to identify genes that may play a role in developing congestive heart failure (CHF) from chemotherapy or other sources. This is an investigational study. All will be enrolled at MD Anderson.


Study summary:

You will have a one time blood draw of 2 teaspoons of blood for use in future research. This blood may be studied in the future to try to find possible genetic or biochemical markers that may be the cause of CHF. Your blood will be drawn either on an outpatient basis or during a routine visit to the hospital. If you already have a central line or an IV placed, the blood will be drawn at these sites to decrease the pain and discomfort of the blood draw. The information obtained in this study will not be put into your medical records.


Criteria:

Inclusion Criteria: - Patients who are at high risk for developing Cardiomyopathy or Congestive Heart Failure. - Patients two months of age and older. Exclusion Criteria: - Those that are not willing to sign an informed consent.


NCT ID:

NCT00500734


Primary Contact:

Principal Investigator
Jean-Bernard Durand, MD
M.D. Anderson Cancer Center

Jean-Bernard Durand, MD
Phone: 713-792-6239
Email: jdurand@mdanderson.org


Backup Contact:

N/A


Location Contact:

Houston, Texas 77030
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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