Testing of an Electronic Patch During Mild Dehydration

Status Completed

Clinical Trial Summary

The purpose of this study is to investigate the ability of a wearable bioimpedance sensor to detect mild dehydration in healthy volunteers following the administration of Furosemide. In addition, the study will investigate changes in bioimpedance related to normal variation in tissue hydration (circadian changes, skin thickness, posture, and moderate activity). The study will also provide information on the durability of the sensor.

Clinical Trial Description

The subjects will use the patches for ten days. During the ten-day period, subjects are exposed to an intervention on day 2 or 3 while being monitored by health personnel: - Subjects are given a diuretic (Furosemide) and monitored for two hours without any intake. - The intervention is followed by intake of a rehydration solution (up to 1500 ml), containing glucose and electrolytes (Resorb Sport, Nestle S.A.). ;

Study Design

Related Conditions & MeSH terms

Dehydration

Clinical Trial Details

NCT number	NCT05129358
Study type	Interventional
Source	Mode Sensors AS
Contact
Status	Completed
Phase	N/A
Start date	May 30, 2022
Completion date	November 3, 2023

View Details

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