Status:

COMPLETED

Evaluation of Hydration Status When Consuming Alkaline Water Compared to Reverse Osmosis Purified Water.

Lead Sponsor:

Natural Immune Systems Inc

Conditions:

Hydration

Eligibility:

All Genders

18-65 years

Phase:

NA

Brief Summary

To conduct a randomized, double-blinded, placebo-controlled, cross-over trial in a population of chronically, moderately dehydrated people comparing two waters on hydration status.

Detailed Description

A randomized, double-blinded, placebo-controlled cross-over study design will be used to evaluate the effects of consumption of alkaline water against reverse osmosis water. The study is of 5 weeks' d...

Eligibility Criteria

Inclusion

  • Adult people of either gender;
  • Age 18 - 65 years (inclusive);
  • BMI between 18.0 and 34.9 (inclusive);
  • Screening results showing at least one of the following:
  • Hematocrit: Women: 45.0 or higher; Men: 48.7 or higher;
  • BUN/Creatinine ratio 20 or higher;
  • Sodium levels 146 mmol/L or higher;
  • Potassium levels 5.3 mmol/L or higher;
  • Chloride levels 108 mmol/L or higher.
  • Willing to maintain a consistent diet (including medications, vitamins and supplements) and lifestyle routine throughout the study;
  • Willing to abstain from coffee, tea, soft drinks, and nicotine for at least one hour prior to a clinic visit;
  • Willing to abstain from alcohol for at least 12 hours prior to a clinic visit;
  • Willing to maintain a consistent habit of abstaining from exercising and nutritional supplements on the morning of a study visit.

Exclusion

  • Cancer during past 12 months;
  • Chemotherapy during past 12 months;
  • Significant active uncontrolled illness (such as lymphoma, liver disease, kidney failure, heart failure).
  • Previous major surgery to stomach or intestines \[(absorption of test product may be altered) minor surgery is not a problem, including appendix and gallbladder removal\];
  • Implanted electronic device such as pacemaker or implantable cardioverter-defibrillator (ICD);
  • Currently experiencing peripheral edema in legs and /or feet;
  • Diagnosed with any blood clotting disorder or taking clotting factor concentrates;
  • Diagnosis of Peripheral Artery Disease;
  • Diagnosis of varicose veins;
  • Currently taking blood pressure medication;
  • Currently taking blood thinning medication (81mg aspirin allowed);
  • Currently taking diuretic medication;
  • Currently taking nutritional supplements and other substances judged by the study coordinator to negate or camouflage the effects of the test product;
  • Women who are pregnant, nursing, or trying to become pregnant.

Key Trial Info

Start Date :

March 1 2020

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 19 2021

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT04460846

Start Date

March 1 2020

End Date

December 19 2021

Last Update

September 27 2022

Active Locations (1)

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NIS Labs

Klamath Falls, Oregon, United States, 97601-5904