Overview
Primary Prevention of Hypertension in Obese Adolescents
Status:
Completed
Completed
Trial end date:
2011-01-01
2011-01-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to examine the consequences of lowering serum uric acid in pre-hypertensive, obese adolescents pathways involved with how uric acid mediated hypertension and renal disease. The specific aims are: 1. Test the hypothesis that lowering uric acid will improve endothelial function. 2. Test the hypothesis that lowering uric acid will reduce plasma renin activity and serum angiotensin II levels. 3. Test the hypothesis that lowering uric acid will reduce markers of inflammationPhase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Collaborator:
Baylor UniversityTreatments:
Allopurinol
Probenecid
Criteria
Inclusion Criteria:Children between the ages of 11 and 18
body mass index greater than the 95th percentile for age
Blood pressure between 75th and 95th percentile for age, gender and height percentile
Exclusion Criteria:
hypertension at the time of screening
allergy to one of the study medications
liver function abnormality (AST or ALT greater than twice the upper limit of
normal for the laboratory)
history of renal stones
renal insufficiency (Schwartz formula calculated GFR less than 70ml per min per 1.73m2 BSA)
positive urine pregnancy test
diabetes
organ transplant recipient
currently treated with an angiotensin converting enzyme inhibitor (ACEI), angiotensin
receptor blocker (ARB), diuretic, other medications known to alter serum uric acid level
lack of ability to comply with the study protocol