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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00397319
Other study ID # 050045
Secondary ID 1422
Status Terminated
Phase N/A
First received November 8, 2006
Last updated July 2, 2007
Start date August 2005
Est. completion date December 2006

Study information

Verified date July 2007
Source Vanderbilt University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

To evaluate specific markers of cardiovascular risk before and after growth hormone replacement therapy in a population of growth hormone deficient adults, as compared to an age, gender, and BMI-matched healthy population.


Description:

Growth hormone deficiency (GHD) is associated with increased cardiovascular morbidity and mortality. The effects of such a deficiency include decreased exercise capacity and tolerance, impaired cardiac function, a central fat redistribution, increased peripheral arterial resistance, and an unfavorable lipid profile. These effects have been found to be reversed with appropriate replacement therapy with recombinant human growth hormone. We plan to utilize several experimental systems to further investigate the role of growth hormone (GH) in maintaining cardiovascular health. In particular, we would like to further understand the interaction of GH with Plasminogen-activator-inhibitor-1 (a major activator of the fibrinolytic system) as well as the role of GH in the maintenance of vascular function.


Recruitment information / eligibility

Status Terminated
Enrollment 26
Est. completion date December 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Adult between the ages of 18 and 65

- Documented Growth Hormone Deficiency as defined by a peak Growth Hormone during a GHRH-Arginine Stimulation test not exceeding 9.5 ng/ml

Exclusion Criteria:

- Personal history of cardiovascular disease (previous myocardial infarction or known coronary artery disease) or diagnosis of heart disease between study visits.

- Personal history of diabetes mellitus or development of diabetes between study visits.

- Initiation of an anti-cholesterol medication or anti-hypertensive between baseline and follow-up study visit.

- Initiation of regular tobacco use between baseline and follow-up study visit.

- Pregnancy or nursing

- Current daily use of any drug known to affect the fibrinolytic system: Aspirin, Aggrenox, Plavix, Persantine, Ticlid, Pletal, Trental, Lovenox, Coumadin, Agrylin, and Hydroxyurea.

Study Design

Observational Model: Case Control, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Drug:
Growth Hormone


Locations

Country Name City State
United States Vanderbilt University Medical Center Nashville Tennessee

Sponsors (3)

Lead Sponsor Collaborator
Vanderbilt University National Center for Research Resources (NCRR), Pfizer

Country where clinical trial is conducted

United States, 

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