Growth Hormone's Effect on Endothelial Progenitor Cells
Completed · Not applicable
Conditions studied: Cardiovascular Disease
In brief
To assess the effect of short-term low-dose growth hormone therapy on the mobilization of endothelial progenitor cells from the bone marrow within a group of healthy adults.
Key facts
- Study ID
- NCT00397592
- Run by
- Vanderbilt University
- People needed
- 18
- Starts
- 2006-08-01
- Expected to finish
- 2007-01-01
- Last updated by the study team
- 2007-07-03
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adults age 18 thru 65
- Serum IGF-1 in the lower half of the age and gender-specific normal range at the time of screening visit
You may not qualify if…
- Systemic hypertension, as defined as current BP >140/90 on screening visit, or taking anti-hypertensive therapy.
- Diabetes mellitus, as defined by known diagnosis or Fasting Blood Glucose >126 at the time of screening visit.
- Women who are pregnant or nursing, as confirmed by history or seum beta-hCG at the time of screening visit.
- Women who are taking exogenous oral estrogens of any kind.
- Personal history of active cancer or recurrence within the past 10 years, with the exception of non-melanoma skin cancer.
- Personal history of an untreated benign intracranial neoplasm.
- Initiation of statin therapy during the course of the study.
- A serum IGF-1 level below the age and gender-specific normal range at the time of screening visit.
- Renal insufficiency, as defined by a GFR <60 mls/min/1.73 m2 upon Renal Function panel at the time of screening visit.
- Hepatic insufficiency, as defined by an AST and/or ALT >twice the upper limit of normal at the time of screening visit.
Where it is running
- Vanderbilt University Medical Center — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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