Actively Recruiting

Phase 4
Age: 35Years - 70Years
All Genders
NCT03471117

Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

Led by The University of Texas at Arlington · Updated on 2025-06-10

28

Participants Needed

2

Research Sites

417 weeks

Total Duration

On this page

Sponsors

T

The University of Texas at Arlington

Lead Sponsor

U

University of Texas, Southwestern Medical Center at Dallas

Collaborating Sponsor

AI-Summary

What this Trial Is About

Chronic kidney disease (CKD) is associated with a higher risk of cardiovascular disease and death. An overactive sympathetic nervous system in CKD patients is one of the major mechanisms increasing the cardiovascular risks in this patient population. Recently, some studies have shown that a drug typically used to improve glucose control (pioglitazone) may also reduce sympathetic nerve activity and improve blood vessel function. The goal of this study is to determine whether a short-term treatment with pioglitazone can reduce sympathetic nerve impulses throughout the body in CKD patients.

CONDITIONS

Official Title

Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

Who Can Participate

Age: 35Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • CKD patients classified as Stage 3 and 4 of National Kidney Foundation Classification with estimated glomerular filtration rate (GFR) between 15 and 59 mL/min/1.73 m2 according to the Modification of Diet in Renal Disease (MDRD) formula based on serum creatinine, age, gender, and race.
  • Men and women 35 to 70 years of age
Not Eligible

You will not qualify if you...

  • Allergy to Glitazones
  • Myocardial infarction
  • Heart failure
  • Angina
  • History of kidney stones
  • Liver disease (abnormal liver enzymes)
  • Anemia (hemoglobin <8 g/dl)
  • Cancer with current treatment
  • Previous organ transplantation
  • Immunosuppressant therapy
  • Human immunodeficiency virus infection
  • Pregnancy or lactating
  • Current tobacco use
  • Dilantin and oral contraceptive usage due to potential drug interaction with glitazones
  • Self-identified history of hypoglycemia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

University of Texas at Arlington

Arlington, Texas, United States, 76010

Actively Recruiting

2

UT Southwestern

Dallas, Texas, United States, 75390

Actively Recruiting

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Research Team

P

Paul J Fadel, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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