Effect of Gemfibrozil on Serum Glycosylphosphatidylinositol (GPI) Phospholipase D and Triglycerides
Completed · Phase 1
Conditions studied: Hypertriglyceridemia
In brief
The purpose of this study is to examine the role of glycosylphosphatidylinositol-specific phospholipase D (GPI-PLD) in triglyceride metabolism.
Key facts
- Study ID
- NCT00108511
- Run by
- US Department of Veterans Affairs
- Starts
- 2004-10-01
- Expected to finish
- 2007-09-01
- Last updated by the study team
- 2009-01-21
Who can join
Age: 19 and older, up to 74. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age >18 and <75
- Fasting triglycerides >150 mg/dl
You may not qualify if…
- Fasting triglycerides >600 mg/dl
- LDL >130 mg/dl
- Concurrent lipid lowering therapy
- Known hypersensitivity to gemfibrozil
- Alcohol intake >30 gm/day (2 drinks/day)
- Fasting glucose >125 mg/dl or known type 2 diabetes
- AST or ALT > 2.0 x upper limit of normal
- Creatinine: men >1.4 mg/dl, women >1.3 mg/dl
- Cancer treatment in the past 5 years (unless cured)
- Infectious diseases including HIV or tuberculosis
- Significant cardiac disease in the past 6 months (myocardial infarction, coronary artery bypass graph, angioplasty, class 3 or 4 congestive heart failure, left bundle branch block, third degree AV block)
- Uncontrolled hypertension (systolic blood pressure [SBP] >180 or diastolic blood pressure [DBP] > 105 mm Hg)
- Anemia (hematocrit <40% men, <35% women)
- Any other significant systemic disease or medication that could interfere with tolerance of medication or outcome
- Any indication that a participant will be unable to adhere to the protocol
- Unable to give informed consent
- Pregnant or breastfeeding females or a female who plans to become pregnant while participating in the study
Where it is running
- Roudebush VA Medical Center — Indianapolis, Indiana, United States
Full record on ClinicalTrials.gov
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