RECRUITING

Effect of Super-Oxygenated Water on Blood Oxygen Saturation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Therapeutic delivery of additional oxygen to blood stream via hyperbaric and extracorporeal oxygenation that raise blood Oxygen saturation level, apart from oxygenation in the lungs, are known to induce tissue repair, restore normal body functions and improve survival. Despite the clinical benefits obtained from these interventions, Oxygen supplementation is rather a medically involved process requiring access to specialized equipment including hyperbaric chambers, cardiac catheterization laboratory and extracorporeal oxygenators, and is not generally amenable for everyday use. The current prospective study will evaluate a non-invasive route for Oxygen delivery through ingestion of super-oxygenated water in adult volunteers. The participants will be randomly assigned to one of the two treatment groups viz. super-oxygenated water or placebo control normal water at 1:1 ratio. Neither the participants nor the study doctor will know the treatment assignment. Pre- and Post-ingestion measurements will be conducted to evaluate effect of super-oxygenated water.

Official Title

A Randomized, Double-blinded and Placebo-controlled Study on Super-Oxygenated Water

Quick Facts

Study Start:2025-05-01
Study Completion:2026-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07016191

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Legally adult (18 years of age or older)
  2. * Subject must be willing to review and provide a written informed consent
  3. * Subject must agree to the study procedures including water ingestion, and SPO2 and heart rate measurements
  1. * Any active and life-threatening medical condition involving hepatic, renal, cardiac, respiratory, endocrine, or gastrointestinal systems, or any blood disorder in view of the Principal Investigator to confound the study
  2. * Female subjects those are pregnant, nursing or planning to become pregnant
  3. * Subjects receiving any experimental medications or have undergone a major surgical procedure in last 30 days
  4. * Subjects are excluded if they have previously utilized the test article (INHALE superoxygenated water) within the last 24 hours, or have undergone bariatric surgery or have received weight-loss medication
  5. * Subjects with known anemia, hemoglobinopathy or other comorbidity necessitating fluid restriction

Contacts and Locations

Study Contact

Ian Mitchell
CONTACT
918-500-2682
ianmitchell81@gmail.com

Principal Investigator

Deepak Nayak, PhD
STUDY_DIRECTOR

Study Locations (Sites)

The Center For Whole Health
Westlake Village, California, 91362
United States

Collaborators and Investigators

Sponsor: Inhale, Inc

  • Deepak Nayak, PhD, STUDY_DIRECTOR

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-05-01
Study Completion Date2026-05

Study Record Updates

Study Start Date2025-05-01
Study Completion Date2026-05

Terms related to this study

Keywords Provided by Researchers

  • Inhale
  • Super-oxygenated Water
  • Superoxygenated Water
  • Blood Oxygen Saturation

Additional Relevant MeSH Terms

  • Adult Volunteers