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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00397319
Date of registration: 08/11/2006
Primary sponsor: Vanderbilt University
Public title: Growth Hormone's Effect on the Cardiovascular System
Scientific title: The Role of Growth Hormone in Cardiovascular Health
Date of first enrolment: August 2005
Target sample size: 26
Recruitment status: Terminated
URL:  http://clinicaltrials.gov/show/NCT00397319
Study type:  Observational
Study design:  Observational Model: Case Control, Time Perspective: Longitudinal, Time Perspective: Prospective  
Countries of recruitment
United States
Contacts
Name:   Doug Vaughan, MD
Address: 
Telephone:
Email:
Affiliation:  Vanderbilt University
Key inclusion & exclusion criteria

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.



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Growth Hormone Deficiency
Intervention(s)
Drug: Growth Hormone
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
050045
1422
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
National Center for Research Resources (NCRR)
Pfizer
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