Viewing Study NCT00185705



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00185705
Status: TERMINATED
Last Update Posted: 2020-03-18
First Post: 2005-09-09

Brief Title: Treatment of Insulin Resistance in Hypertensive Obese Adolescents
Sponsor: Stanford University
Organization: Stanford University

Study Overview

Official Title: Randomized Placebo Controlled Double Blind Trial of Telmisartan in Hypertensive Obese Adolescents
Status: TERMINATED
Status Verified Date: 2020-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Primary investigator moved to different university
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In this study we propose using telmisartan an angiotensin II receptor antagonist with PPAR-gamma modulating activity for a 12-week period to decrease blood pressure and insulin levels in obese hypertensive children Telmisartan is currently approved for treatment of adult hypertension Recent adult studies however have shown telmisartan as an effective medication for lowering insulin levels and improving insulin sensitivity We will enroll 30 obese adolescents ages 10 to 18 years and randomly assign half of the group to receive telmisartan and the other half to receive placebo sugar-pill We will obtain fasting glucose and insulin levels as well as other markers for insulin sensitivity and cholesterol panel at the beginning of the study at each clinic visit in 4-week intervals and at the end of the study We will obtain an imaging study computed tomography CT scan on 10 randomly selected study patients 5 from each group to examine the distribution of fat tissue before and after treatment Studies suggest that fat tissue in the subcutaneous tissue is less harmful that fat tissues surrounding internal organs such as the liver We will also provide nutritional handouts and exercise recommendations to each participant as a life-style intervention Each participant will be given a diary to record his or her diet and exercise activities throughout the study
Detailed Description: Hypothesis This pilot study will provide data essential for designing a larger trial to test the hypothesis that telmisartan treatment of obese children with insulin resistance and hypertension will result in improved insulin levels and systolic blood pressure Secondary outcome measures will include the effects of telmisartan on total cholesterol triglyceride HDL and LDL levels body mass index BMI and body fat distribution

Specific Aims for to Test Hypothesis

Aim 1 Determine the change in insulin sensitivity in adolescents with obesity and hyperinsulinemia before and after treatment with telmisartan We hypothesize a significant increase in insulin sensitivity following medical treatment We will measure fasting insulin and glucose levels for calculation of the homeostasis model assessment HOMA 29 30 Furthermore we will calculate parameters of insulin production and insulin resistance from simultaneous measurements of glucose insulin and C-peptide levels during an oral glucose tolerance test OGTT We will check IGF BP-1 insulin-like growth factor 1 binding protein level as an indirect measurement of insulin resistance Due to the risks associated with glucose clamps and continuous insulin infusion we will not use this procedure in our study

Aim 2 Determine the change in systolic blood pressure in adolescents with obesity and hypertension before and after treatment with telmisartan We hypothesize a significant decrease in systolic blood pressure following medical treatment Subjects will have blood pressure checked at each clinic visit

Aim 3 Evaluate changes in lipid profile and body mass index as secondary outcome measures with telmisartan treatment Subjects will have weight height and fasting lipid panel checked at each clinic visit

Aim 4 Characterize fat distribution before and after telmisartan treatment A subset of study participants will undergo magnetic resonance imaging MRI to characterize and separate abdominal adipose tissue into its subcutaneous and visceral components A one-slice MRI will be obtained at 2 time-points during the study weeks 0 and 12

Aim 5 Determine the feasibility of using telmisartan for the treatment of hyperinsulinemia and hypertension in obese adolescents Study results will provide necessary data to calculate the power needed for a multi-center randomized placebo-controlled trial of telmisartan

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None