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AVACEN Treatment Method and Postprandial Blood Glucose

Postprandial Hyperglycemia Clinical Trial

Official title:
AVACEN Treatment Method and Postprandial Blood Glucose

Clinical Trial Summary

A double-blind crossover randomized controlled trial to investigate the effects of the AVACEN device on postprandial blood glucose. The AVACEN device creates negative pressure around the hand while heating the palm. Two sham devices, one providing heat but no vacuum and one providing neither heat nor vacuum were also used. Each subject will use each of these three devices during the first hour of a 2-hour oral glucose tolerance test on separate visits. Subjects arrived in the morning following an overnight fast. Fasting blood glucose, blood pressure, tympanic temperature, and subjective thermal ratings were measured before and throughout the 2-hour oral glucose tolerance test.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04018976
Study type Interventional
Source San Diego State University
Contact
Status Completed
Phase N/A
Start date May 5, 2019
Completion date September 15, 2019
View Details
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