Calcium Channel Splice Variant Expression in Cardiovascular Disease and Aging
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Purpose
The purpose of this study is to learn what changes in blood vessel contraction may occur as a result of a disease of the vessel that requires surgery. The study will examine the calcium channels present in the vessels being operated on, and the genes that may alter blood vessel function. Possible variation in these genes may change the kind of calcium channels present in blood vessels.
| Condition |
|---|
|
Atherosclerosis |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Cross-Sectional |
| Official Title: | Calcium Channel Splice Variant Expression in Cardiovascular Disease and Aging |
Vascular tissue obtained from the surgical site that would have otherwise been discarded and Blood Serum
| Enrollment: | 18 |
| Study Start Date: | August 2012 |
| Study Completion Date: | August 2012 |
| Primary Completion Date: | August 2012 (Final data collection date for primary outcome measure) |
The goal of this study is to learn more about how blood vessels function and the mechanism that causes them to contract. The study will investigate the natural history of diseased blood vessel tissue and the calcium channels in the muscle part of the blood vessel. The study will also examine how genetics influences cardiovascular disease and its causes and treatments.
Patients scheduled for vascular surgery will be approached to participate in this study. During surgery, tissue fragments of diseased and marginal tissue will be obtained. A blood sample will be obtained at either the time of surgery or consent and genomic DNA will be extracted.
Eligibility| Ages Eligible for Study: | 21 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Patients scheduled for vascular surgery
Inclusion Criteria:
- Ages 21 and older
- Scheduled for vascular surgery
Exclusion Criteria:
- Unwillingness to be subjected to diagnostic and/or therapeutic procedures that are deemed not necessary for clinical management
- Volunteers deemed too fragile to participate in the study by the principal investigator (PI) or the attending physician
- Inability to obtain informed consent from either the volunteer or the responsible party (durable power of attorney [DPA]) for the volunteer, with the volunteer's assent
Contacts and Locations| United States, Maryland | |
| National Institute on Aging, Harbor Hospital | |
| Baltimore, Maryland, United States, 21225 | |
| Principal Investigator: | Samer Najjar, MD | National Institute on Aging (NIA) |
More Information
Publications:
| Responsible Party: | National Institutes of Health Clinical Center (CC) ( National Institute on Aging (NIA) ) |
| ClinicalTrials.gov Identifier: | NCT00251615 History of Changes |
| Other Study ID Numbers: | AG0058 |
| Study First Received: | November 8, 2005 |
| Last Updated: | August 3, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institutes of Health Clinical Center (CC):
|
vascular surgery vascular aging arterial aging surgical tissue Aging |
Additional relevant MeSH terms:
|
Atherosclerosis Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases |
ClinicalTrials.gov processed this record on May 22, 2013