Biorepository: Indiana Health Study (IHS)
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Purpose
Blood samples and health information (e.g., age at diagnosis, test results) are collected for the purposes of genetic research. The blood samples are assigned a number and stored in a repository for safe keeping until they are needed for a research project. Participants are persons who are healthy (not having high blood pressure, diabetes, or high cholesterol levels) or persons who have Coronary Artery Disease (CAD) and live in Indiana. Participants complete a questionnaire at the time the blood sample is drawn and are contacted once a year to update their health history. Researchers apply to the Fairbanks Institute for use of the blood samples and health information minus participant names and contact information. Their research is required to be related to find genes or substances made by genes that may be involved in Coronary Artery Disease with the purpose of improving the investigators understanding of the illness potentially leading to the development of new diagnostic tools for identifying the illness, new treatments,or preventative measures. This study will be repeated for other disorders like Diabetes and Cancer.
| Condition |
|---|
|
Coronary Artery Disease Heart Disease Healthy |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Collection and Storage of Human Biological Materials (Blood Sample) and Linked Phenotypic Information (Health History) for Research Purposes |
70ml of whole blood: 3-10 ml EDTA tubes for collection of whole blood 3-10 ml SST tubes (red tops) for collection of serum 2-3ml PAXgene tubes for collection of RNA A minimum of 1 EDTA and 1 SST tube is required for enrollment into the study.
| Estimated Enrollment: | 1400 |
| Study Start Date: | June 2008 |
| Estimated Study Completion Date: | June 2013 |
| Estimated Primary Completion Date: | December 2012 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
|
Case
Those with a diagnosis of Coronary Artery Disease
|
|
Control
Those who do not have Coronary Artery Disease (are healthy) but are matched to a Case participant by age, gender, and ethnicity.
|
Detailed Description:
Study Aim:
The purpose of this study is to create an extensively annotated bio-repository platform for hypothesis-driven research that will lead to advancements in the diagnosis, treatment and prevention of diseases common to the population of Indiana. The first phase of this research platform will be created by collecting blood samples from two groups of individuals in the Central Indiana community, one with documented evidence of coronary artery disease (CAD), and a second group of age, gender and ethnicity matched individuals without clinical evidence of CAD. Each individual's blood sample will be linked to their clinical, demographic and epidemiological information, gathered both retrospectively and prospectively. This will be repeated with individuals who have Cancer, Diabetes and potentially other illnesses.
Recruitment:
This initial study will include 750 individuals with CAD (the CAD Group) and 750 individuals who are age, gender, and ethnicity matched to the CAD Group, but without presentation of clinical evidence of CAD (the Control Group). To reflect the growing representation of Hispanics in Central Indiana, Hispanics will be overly recruited in both groups so that the study population accurately reflects the general population of Central Indiana.
Follow-up:
As this is a prospective, longitudinal study, follow-up of study subjects is intended to continue indefinitely, unless, of course, at any time, consent for further follow-up is withdrawn by the subject. Follow-up will include continuing access to the subject's medical record, as well as facilitating continued contact by telephone, to pursue data concerning changes in the subject's health. Subjects may be contacted by telephone, mail or email every twelve months to ask if they wish to continue participation in the study.
The collected dataset (made up of the collected blood samples linked to clinical and epidemiological information collected retrospectively and prospectively), will be used in medical research to find genes, or gene products such as RNA or proteins that will help in understanding the causes of disease and will guide the development of new treatments.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
This initial study will include 750 individuals with CAD (the CAD Group) and 750 individuals who are age, gender, and ethnicity matched to the CAD Group, but without presentation of clinical evidence of CAD (the Control Group). To reflect the growing representation of Hispanics in Central Indiana, Hispanics will be overly recruited in both groups so that the study population accurately reflects the general population of Central Indiana.
Inclusion Criteria:
1. Study subjects will be recruited for the CAD group based on a history confirmed by the medical record of at least one of the following:
- Angioplasty, with or without stent placement
- Coronary Artery Bypass Graft (CABG) surgery
- Diagnostic angiogram or positive catheterization results showing 50% occlusion or greater
Exclusion Criteria:
Study subjects for the Control Group will be excluded based on a confirmed history of:
- CAD as defined above, or as history of a positive stress test for ischemia, Troponin > 0.5 or myocardial infarction
- Diabetes (type 1 or 2)
- Hypertension (confirmed with at least two documented measurements of blood pressure greater than 140/90, not attributed to treating medications)
- Abnormal lipid profile defined as LDL-C < 130mg/dl, HDL ≥ 40 mg/dl, cholesterol < 240 mg/dl or triglycerides < 200 mg/dl
- Patients taking any medications commonly used for the above excluded conditions
- History of stroke or Transient Ischemic Attacks (TIAs)
Exclusion criteria for both the CAD Group and the Control Group will be a known or reported history of:
- Hepatitis B
- Hepatitis C
- AIDS (HIV positive)
- Tuberculosis
- Cancer (including melanoma, but excluding low-malignancy skin cancer)
- Non-autologous bone marrow transplant
- Blood transfusion within 120 days
- In addition, prisoners, minors, patients requiring the consent of a caregiver or Authorized Representative, and/or any subjects deemed medically unsuitable for research donation by their treating physician (for reasons such as anemia, hematopoetic disorders/cancers or low body weight) will be excluded from the study.
- Subjects unwilling to consent to the allowance of future follow-up will be excluded from initial participation.
Contacts and Locations| Contact: Mary Ann Caldwell, RNC CCRC | 317-274-8915 | macaldwe@iupui.edu |
| Contact: Brooke McMillen | 317-238-2483 | bmcmillen@fairbanksinstitute.org |
| United States, Indiana | |
| American Health Network | Recruiting |
| Avon, Indiana, United States | |
| Contact: Carla Cravens 317-745-8000 ext 453 carla_cravens@ahni.com | |
| Principal Investigator: Mary Schmoll, NP | |
| Investigator's Research Group | Recruiting |
| Brownsburg, Indiana, United States | |
| Contact: Rod Rapheal 317-297-7999 investigatorsresearch@yahoo.com | |
| Principal Investigator: Kenneth Maynard, DO | |
| American Health Network | Recruiting |
| Franklin, Indiana, United States | |
| Contact: Michelle Meier, LPN 317-738-7448 michelle_Meier@ahni.com | |
| Contact: Christine Wathen 317-738-7448 Christine_wathen@ahni.com | |
| Principal Investigator: Jill Beavins, MD | |
| American Health Network | Recruiting |
| Greenfield, Indiana, United States | |
| Contact: Vickie McDaniel, LPN 317-462-5252 ext 248 vickie_mcdaniel@ahni.com | |
| Principal Investigator: Stephanie Kinnaman, MD | |
| Indiana Heart Hospital: Community Heart and Vascular Clinic | Recruiting |
| Indianapolis, Indiana, United States, 46219 | |
| Contact: Brenda Neuman, LPN 317-621-8628 bneuman@ecommunity.com | |
| Principal Investigator: DeoVrat Singh, MD | |
| Outpatient Clinical Research Facility/Indiana Cancer Pavilion | Recruiting |
| Indianapolis, Indiana, United States, 46202 | |
| Contact: Mary Ann Caldwell, RNC CCRC 317-554-5790 macaldwe@iupui.edu | |
| Contact: Brooke McMillen 317-238-2483 bmcmillen@fairbanksinstitute.org | |
| Principal Investigator: Anantha Shekhar, MD PhD | |
| Krannert Institute of Cardiology/IU Dept. of Medicine | Recruiting |
| Indianapolis, Indiana, United States, 46202 | |
| Contact: Jeri L Steward 317-962-0080 steward3@iupui.edu | |
| Sub-Investigator: Jacquelyn o'Donnell, MD | |
| Alivio Medical Center (spanish/espaniol) | Recruiting |
| Indianapolis, Indiana, United States, 46222 | |
| Contact: Jorge Ayala 317-635-3499 jorfa@insightbb.com | |
| Contact: Alfredo Lopez, MD 317-635-3499 | |
| Principal Investigator: Alfredo Lopez, MD | |
| Oral Health Research Institute | Recruiting |
| Indianapolis, Indiana, United States | |
| Contact: Melissa Mau 317-274-5439 mmau@iupui.edu | |
| Principal Investigator: Ana Gossweiler | |
| American Health Network | Active, not recruiting |
| Indianapolis, Indiana, United States, 46254 | |
| Corvasc MDs | Recruiting |
| Indianapolis (North), Indiana, United States | |
| Contact: Sara Gallagher 317-583-7804 sgallagher@corvascmds.com | |
| Principal Investigator: Christopher Salerno, MD | |
| Indiana Heart Physicians | Recruiting |
| Indianapolis (South), Indiana, United States | |
| Contact: Molly Miller 317-893-1900 molly.miller@ssfhs.org | |
| Principal Investigator: Carl Rouch, MD | |
| IU Health Arnett | Recruiting |
| Lafayette, Indiana, United States | |
| Contact: Stephanie Middleton 765-448-8019 smiddle3@clarianarnett.com | |
| Principal Investigator: Dona Gray, MD | |
| Medical Consultants, PC | Recruiting |
| Muncie, Indiana, United States | |
| Contact: Sherri Adair 765-254-4761 | |
| Principal Investigator: Bruce Graham, MD | |
| Principal Investigator: | Anantha Shekhar, MD PhD | Indiana University School of Medicine/CTSI |
| Study Director: | Cynthia Helphingstine, PhD | Fairbanks Institute for Healthy Communities |
More Information
Additional Information:
No publications provided
| Responsible Party: | Cynthia J. Helphingstine, Fairbanks Institute for Healthy Communities |
| ClinicalTrials.gov Identifier: | NCT00741416 History of Changes |
| Other Study ID Numbers: | FI-08-US-0001 |
| Study First Received: | August 25, 2008 |
| Last Updated: | June 30, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Fairbanks Institute:
|
Heart Disease Biorepository Biobank |
Additional relevant MeSH terms:
|
Coronary Artery Disease Myocardial Ischemia Coronary Disease Heart Diseases |
Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases |
ClinicalTrials.gov processed this record on May 21, 2013