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RECRUITING
NCT04715022
PHASE1/PHASE2

Sympathetic-vascular Dysfunction in Obesity and Insulin Resistance (Vitamin C Study)

Sponsor: University of Kansas Medical Center

View on ClinicalTrials.gov

Summary

The main purpose of research is to examine and understanding the development of hypertension in obese adults with insulin resistance. Findings from our studies will identify unique mechanisms that can be targeted to limit increases in vascular dysfunction and reduce the excessively high prevalence of hypertension and risk for cardiovascular disease (CVD). This study is testing the health of the blood vessels and the activity of the nerves that control the blood vessels in adults with insulin resistance. The extent to which ascorbic acid (Vitamin C) improves the function of the blood vessels will be determined. The primary outcome is blood pressure, which is the result of blood vessel health and activity of the nerves, and the reduction in blood pressure that is observed with ascorbic acid.

Official title: Sympathetic-vascular Dysfunction in Obesity and Insulin Resistance

Key Details

Gender

All

Age Range

35 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

23

Start Date

2021-06-17

Completion Date

2027-08-01

Last Updated

2025-06-08

Healthy Volunteers

No

Interventions

DRUG

Ascorbic acid solution (American Regent Laboratories Inc.)

Ascorbic acid solution (American Regent Laboratories Inc.) will be obtained from the KU Investigational Pharmacy located in the KU Clinical Research Center where studies will take place. A priming bolus of 0.06 g ascorbic acid/kg fat free mass (FFM) dissolved in 100 mL of saline will be infused intravenously at 5 mL/min for 20 minutes, followed immediately by a "drip-infusion" of 0.02 g/kg FFM dissolved in 30 mL of saline administered over 2 hours at 0.5 mL/min.

DRUG

Saline

Placebo (saline) will be administered

Locations (1)

University of Kansas Medical Center

Kansas City, Kansas, United States