Mitigating the Pro-inflammatory Phenotype of Obesity

Trial statusRecruiting
Trial phasePhase 1
Trial typeInterventional
Biological sexAll
Age18-79
SponsorUniversity of Kansas Medical Center

About this trial

The purpose of this study is to examine the hypothesize that 4 weeks of sympathetic nerve activity (SNA) inhibition (oral clonidine) will cause a significant reduction in circulating blood concentrations and endothelial cell expression of inflammatory markers (e.g., TNF-α, IL-6).

Our study is a prospective study using a randomized, double-blinded design to test 4 weeks of SNA blockade (oral clonidine) compared with a BP-lowering control condition (diuretic, hydrochlorothiazide) or a placebo.

Eligibility criteria

Qualifiers

Male or Female, age 18-79

Obese: BMI > 30 m/kg2

Hypertensive: blood pressure >130/80

Elevated insulin resistance (HOMA-IR > 2.5)

Disqualifiers

Current use of clonidine or beta-blockers

Current smoker or History of smoking in the past 3 months.

Hyperlipidemia: Fasting triglycerides > 250 mg/dL

Currently taking hypertension medication

Trial design

Treatments tested in this trial

  • Hydrochlorothiazide 12.5Mg Tab
  • Clonidine Pill
  • Placebo

Treatment groups

60 Participants
are divided into 3 treatment groups