DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more



Evaluating the Link Between Thiazide Medications, the Nervous System, and Diabetes in Individuals With High Blood Pressure

Information source: University of Texas Southwestern Medical Center
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Hypertension

Intervention: Chlorthalidone (Drug); Spironolactone (Drug); Eplerenone (Drug); Quinapril (Drug); Irbesartan (Drug)

Phase: Phase 4

Status: Completed

Sponsored by: University of Texas Southwestern Medical Center

Official(s) and/or principal investigator(s):
Wanpen Vongpatanasin, MD, Principal Investigator, Affiliation: University of Texas Southwestern Medical Center at Dallas

Summary

Thiazide medications are often prescribed for individuals with high blood pressure, but research has shown that they may increase an individual's risk of developing diabetes. While it is unknown exactly how thiazide causes this response, it is likely that the nervous system is somehow involved. This study will evaluate the role of the nervous system in sugar metabolism, as well as determine the effect of thiazide and other medications on individuals with high blood pressure.

Clinical Details

Official title: Neural Mechanisms of Thiazide-induced Insulin Resistance

Study design: Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Primary outcome:

Sympathetic Nerve Activity

24-hour Ambulatory Blood Pressure

Insulin Sensitivity

Forearm Blood Flow

Baroreflex Sensitivity

C-reactive Protein

Inflammatory Cytokines

Secondary outcome:

Electrolytes

Body Weight

Detailed description: Thiazide medications, including chlorthalidone, are commonly prescribed for individuals with high blood pressure because they are inexpensive, effective at lowering blood pressure, and able to reduce the risk of heart failure and stroke. Despite these advantages, research has shown that thiazide medications may increase an individual's risk of developing diabetes. The exact mechanism that causes this remains unknown. Thiazide appears to increase sympathetic nervous system activity, thereby decreasing glucose reuptake and metabolism by skeletal muscle tissues. In turn, this tends to contribute to glucose intolerance and the development of diabetes. More research, however, is needed to confirm this link. Spironolactone, another blood pressure medication, does not pose the same risk for developing diabetes and may prove beneficial as a primary treatment for high blood pressure. The purpose of this study is to determine the role of the sympathetic nervous system in glucose metabolism in individuals with high blood pressure, as well as compare the effectiveness of thiazide, spironolactone, and other antihypertensive medications in reducing blood pressure. Results from this study may initiate the development of future clinical trials involving spironolactone as a primary treatment for reducing blood pressure. This study will enroll individuals with high blood pressure. Participants will be assigned to one of eight treatment groups. Depending on the assigned group, participants will receive chlorthalidone, spironolactone, quinapril, irbesartan, eplerenone, or a combination of these drugs, with or without placebo. Participants will attend four to six study visits over a period of 16 to 28 weeks. All participants will attend a baseline study visit, which will include a physical examination, a medical history review, vital sign measurements, and blood and urine collection. Small electrodes will be used to measure muscle nerve activity. In addition, blood pressure will be monitored continuously for 24 hours prior to the start of the study. Depending on the assigned treatment group, study visits may include blood collection, blood pressure monitoring, an electrocardiogram (ECG) to record heart activity, nerve function monitoring, and/or plasma volume measurements. Participants' baroreflex sensitivity may also be measured by monitoring nerve ending responses within the heart and blood vessels. Insulin sensitivity will be measured with a glucose tolerance test and by evaluating skeletal muscle glucose uptake.

Eligibility

Minimum age: 18 Years. Maximum age: 65 Years. Gender(s): Both.

Criteria:

Inclusion Criteria:

- Untreated stage 1 primary hypertension (systolic blood pressure between 140 to 159 mm

Hg and diastolic blood pressure between 90 to 99 mm Hg) Exclusion Criteria:

- Cardiopulmonary disease, as determined by medical history or by physical examination

- Serum creatinine greater than or equal to 1. 5 mg/dL

- Diabetes mellitus or other systemic illness

- Left ventricular hypertrophy by echocardiography or ECG

- Hypersensitivity to chlorthalidone, spironolactone, eplerenone, angiotensin

converting enzyme (ACE) inhibitors, angiotensin receptor blocker, insulin, Evans blue dye, or clonidine

- History of substance abuse (other than tobacco)

- History of gouty arthritis

- History of ACE inhibitor-induced cough or angioedema

- Evidence of secondary hypertension

- Pregnant

Locations and Contacts

University of Texas Southwestern Medical Center, Dallas, Texas 75390, United States

University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390, United States

Additional Information

Starting date: January 2005
Last updated: December 16, 2014

Page last updated: August 23, 2015

-- advertisement -- The American Red Cross
 
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2017