Pioglitazone to Reduce Sympathetic Overactivity in CKD Patients

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age35-70
SponsorThe University of Texas at Arlington

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Allergy to Glitazones

Myocardial infarction

Heart failure

Angina

Trial design

Treatments tested in this trial

  • Pioglitazone
  • Placebo

Treatment groups

28 Participants
are divided into 2 treatment groups

Sponsors and collaborators

The University of Texas at Arlington

Lead sponsor

University of Texas, Southwestern Medical Center at Dallas

Collaborator