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Clinical Trials/NCT03846141
NCT03846141
Completed
Not Applicable

Hydrogen Inhalation for Health and Exercise Performance

University of Novi Sad, Faculty of Sport and Physical Education1 site in 1 country20 target enrollmentJanuary 15, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Exercise Performance
Sponsor
University of Novi Sad, Faculty of Sport and Physical Education
Enrollment
20
Locations
1
Primary Endpoint
Change in exercise performance
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

In this randomized double-blind, placebo-controlled, crossover pilot trial, we evaluated the effects of 7-day H2 inhalation on exercise performance outcomes and serum hormonal and inflammation profiles in a cohort of young men and women.

Detailed Description

All participants were allocated to receive either gaseous hydrogen (4%) or placebo (room air) by 20-min once-per-day inhalation for 7 days, with wash-out period of 7 days to prevent the residual effects of interventions across study periods. The primary treatment outcome was the change in running time-to-exhaustion from baseline to day 7. Additionally, assessment of other exercise performance endpoints and clinical chemistry biomarkers were performed at baseline and after 7 days after each intervention.

Registry
clinicaltrials.gov
Start Date
January 15, 2018
End Date
September 15, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Novi Sad, Faculty of Sport and Physical Education
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 -35 years Body mass index 20 - 25 kg/m2 Free of major diseases Physically active Must be able to give written informed consent

Exclusion Criteria

  • Use of any dietary supplements within 4 weeks before study commences Abnormal values for lab clinical chemistry (\> 2 SD)

Outcomes

Primary Outcomes

Change in exercise performance

Time Frame: Change from baseline running time-to-exhaustion at 7 days

Running time-to-exhaustion

Secondary Outcomes

  • Change in exercise performance(Change from baseline maximal voluntary isometric strength at 7 days)
  • Change in clinical chemistry biomarker(Change from baseline serum ghrelin at 7 days)

Study Sites (1)

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