Skip to content

Dehydration, Rehydration, and Blood Viscosity

Randomized, Double-blind, Parallel Arm Study of the Effect of Essentia Water, an Electrolyzed High-pH Bottled Water, on Serial Blood Viscosity and Other Hydration Biomarkers in Healthy Subjects

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02118883
Enrollment
100
Registered
2014-04-21
Start date
2014-04-30
Completion date
2014-07-31
Last updated
2014-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dehydration

Keywords

exercise, hydration, dehydration, rehydration, alkaline water, blood viscosity, plasma osmolality, bioimpedance

Brief summary

The purpose of this study is to examine and compare the rehydration effect of Essentia Water, an electrolyzed high-pH bottled water, with industry-standard bottled water purified by reverse osmosis with minerals added, on (1) whole blood viscosity, (2) plasma osmolality, (3) bioelectrical impedance analysis, and (4) body mass change, using serial measurements in apparently healthy adults following exercise-induced dehydration in a controlled environment.

Interventions

OTHEREssentia Water
OTHERBottled water

Sponsors

Health Onvector Inc.
CollaboratorINDUSTRY
Essentia Water, LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
25 Years to 49 Years
Healthy volunteers
Yes

Inclusion criteria

* Free from any medication for at least 1 week prior to the study

Exclusion criteria

* Any chronic condition requiring regular treatment or medical follow-up * Bleeding disorder or susceptible to prolonged or uncontrolled bleeding * Active infection * Current smoker * Subject has a BMI equal or greater than 30 * Use of oral contraceptives in the previous 3 months * Subject is pregnant or breast-feeding * Currently menstruating

Design outcomes

Primary

MeasureTime frameDescription
Change in whole blood viscosity from dehydrated state120 min following rehydrationBlood viscosity measured using a scanning capillary viscometer

Secondary

MeasureTime frameDescription
Change in whole blood viscosity from dehydrated state15, 30, 60, and 90 min following rehydrationBlood viscosity measured using scanning capillary viscometer
Change in plasma osmolality from dehydrated state15, 30, 60, 90, and 120 min following rehydrationPlasma osmolality measured using freezing point osmometer
Change in bioelectrical impedance45, 75, and 120 min following rehydrationImpedance is measured to provide an estimation of body composition using a bioelectrical impedance analyzer (RJL Quantum IV).
Body mass change45, 75, and 120 min following rehydration

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026