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The Effects of Hydrogen-rich Formulation for Treatment of Sport-related Soft Tissue Injuries

Primary Purpose

Soft Tissue Injuries

Status
Completed
Phase
Phase 2
Locations
Serbia
Study Type
Interventional
Intervention
HYDRO
ACTIVE
HYDRO 2
Sponsored by
Center for Health, Exercise and Sport Sciences, Serbia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Soft Tissue Injuries focused on measuring Inflammation, Pain intensity, Flexibility, RICE protocol, Swelling

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • recent history of acute soft-tissue sports injury
  • professional athletes

Exclusion Criteria:

  • not ambulatory patients
  • clinical findings classed as more severe than grade II

Sites / Locations

  • Center for Health, Exercise and Sport Sciences

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Experimental

Arm Label

HYDRO 2

ACTIVE

HYDRO

Arm Description

Subjects in the second experimental group will follow the procedures of first experimental group with additional administration of hydrogen-rick packs 6 times per day for 20 minutes throughout the study.

During the period of 2 weeks subjects will receive traditional treatment protocol after the soft-tissue injury, consisting of RICE protocol during the first 48 h (e.g. rest, ice packs for 20 minutes every 2 hours, compression with elastic bandage, elevation of the injured area above the level of the heart at all possible times) and sub-acute protocol thereafter (e.g. passive stretching 3 times per day for 90 sec, isometric strength exercise with 3 sets with 15 repetitions, 30 min of pain-free weight-bearing exercise).

Subjects in the first experimental group will follow the PLA procedures with additional administration of oral hydrogen-rich capsules (4 capsules three times per day) throughout the study.

Outcomes

Primary Outcome Measures

change in serum C-reactive protein

Secondary Outcome Measures

change in pain intensity during rest and walking

Full Information

First Posted
December 25, 2012
Last Updated
September 27, 2013
Sponsor
Center for Health, Exercise and Sport Sciences, Serbia
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1. Study Identification

Unique Protocol Identification Number
NCT01759498
Brief Title
The Effects of Hydrogen-rich Formulation for Treatment of Sport-related Soft Tissue Injuries
Study Type
Interventional

2. Study Status

Record Verification Date
September 2013
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
June 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Center for Health, Exercise and Sport Sciences, Serbia

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Since hydrogen therapy in humans seems to be beneficial for treating inflammation, ischemia-reperfusion injury and oxidative stress, it seems plausible to evaluate the effects of exogenously administered hydrogen as an element of instant management of sport-related soft tissue injuries (e.g. muscle sprain, ligament strain, tendonitis, contusion). The main aim of the present study will be to examine the effects of two-week hydrogen-rich oral and topical administration on the inflammation, recovery and functional abilities in competitive male and female athletes after acute soft-tissue injury. During the season 2012/2013 (from February to June) subjects (36 professional athletes) will be recruited and examined by certified sports medicine specialist in the out-patient clinics of the Center for Health, Exercise and Sport Sciences in the first 24 hours after the sport-related soft tissue injury was sustained. The subjects will be allocated to a double-blind design to three randomly assigned trials. During the period of 2 weeks subjects in the placebo group (PLA) will receive traditional treatment protocol after the soft-tissue injury, consisting of RICE protocol during the first 48 h and sub-acute protocol thereafter. Subjects in the first experimental group will follow the above procedures with additional administration of oral hydrogen-rich capsules (4 capsules three times per day) throughout the study. Subjects in the second experimental group will follow the procedures of first experimental group with additional administration of hydrogen-rick packs 6 times per day for 20 minutes throughout the study. Participants will be evaluated at the beginning of the study (e.g. at the time of the injury report), after 7 and 14 days after baseline testing for: a) serum C-reactive protein, plasma viscosity and interleukin 6 level, b) pain intensity during rest and walking, c) degree of joint swelling, d) passive joint flexibility, and, e) subjective side-effects. The investigators expect that the administration of hydrogen will significantly improve inflammation outcomes (e.g. decrease in serum C-reactive protein) as compared to the placebo, with topical hydrogen administration will additionally improve post-injury recovery outcomes (e.g. pain intensity, degree of swelling). These results could support the hypothesis that hydrogen-rich intervention may be included as an element of immediate treatment for sport-related soft tissue injuries.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Soft Tissue Injuries
Keywords
Inflammation, Pain intensity, Flexibility, RICE protocol, Swelling

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
36 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HYDRO 2
Arm Type
Experimental
Arm Description
Subjects in the second experimental group will follow the procedures of first experimental group with additional administration of hydrogen-rick packs 6 times per day for 20 minutes throughout the study.
Arm Title
ACTIVE
Arm Type
Active Comparator
Arm Description
During the period of 2 weeks subjects will receive traditional treatment protocol after the soft-tissue injury, consisting of RICE protocol during the first 48 h (e.g. rest, ice packs for 20 minutes every 2 hours, compression with elastic bandage, elevation of the injured area above the level of the heart at all possible times) and sub-acute protocol thereafter (e.g. passive stretching 3 times per day for 90 sec, isometric strength exercise with 3 sets with 15 repetitions, 30 min of pain-free weight-bearing exercise).
Arm Title
HYDRO
Arm Type
Experimental
Arm Description
Subjects in the first experimental group will follow the PLA procedures with additional administration of oral hydrogen-rich capsules (4 capsules three times per day) throughout the study.
Intervention Type
Dietary Supplement
Intervention Name(s)
HYDRO
Intervention Type
Dietary Supplement
Intervention Name(s)
ACTIVE
Intervention Type
Dietary Supplement
Intervention Name(s)
HYDRO 2
Primary Outcome Measure Information:
Title
change in serum C-reactive protein
Time Frame
every week, up to 2 weeks
Secondary Outcome Measure Information:
Title
change in pain intensity during rest and walking
Time Frame
every week, up to 2 weeks
Other Pre-specified Outcome Measures:
Title
change in degree of joint swelling
Time Frame
every week, up to 2 weeks
Title
change in passive joint flexibility
Time Frame
every week, up to 2 weeks
Title
change in plasma viscosity
Time Frame
every week, up to 2 weeks
Title
change in serum interleukin 6
Time Frame
every week, up to 2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: recent history of acute soft-tissue sports injury professional athletes Exclusion Criteria: not ambulatory patients clinical findings classed as more severe than grade II
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sergej M Ostojic, MD, PhD
Organizational Affiliation
Center for Health, Exercise and Sport Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Health, Exercise and Sport Sciences
City
Belgrade
ZIP/Postal Code
11000
Country
Serbia

12. IPD Sharing Statement

Citations:
PubMed Identifier
22560529
Citation
Ostojic SM. Serum alkalinization and hydrogen-rich water in healthy men. Mayo Clin Proc. 2012 May;87(5):501-2. doi: 10.1016/j.mayocp.2012.02.008. No abstract available.
Results Reference
background
PubMed Identifier
18191749
Citation
Jackson MJ. Free radicals generated by contracting muscle: by-products of metabolism or key regulators of muscle function? Free Radic Biol Med. 2008 Jan 15;44(2):132-41. doi: 10.1016/j.freeradbiomed.2007.06.003. Epub 2007 Jun 13.
Results Reference
background
PubMed Identifier
22720117
Citation
Ohno K, Ito M, Ichihara M, Ito M. Molecular hydrogen as an emerging therapeutic medical gas for neurodegenerative and other diseases. Oxid Med Cell Longev. 2012;2012:353152. doi: 10.1155/2012/353152. Epub 2012 Jun 8.
Results Reference
background
PubMed Identifier
25295663
Citation
Ostojic SM, Vukomanovic B, Calleja-Gonzalez J, Hoffman JR. Effectiveness of oral and topical hydrogen for sports-related soft tissue injuries. Postgrad Med. 2014 Sep;126(5):187-95. doi: 10.3810/pgm.2014.09.2813.
Results Reference
derived

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The Effects of Hydrogen-rich Formulation for Treatment of Sport-related Soft Tissue Injuries

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