Clinical Trials Directory

Trials / Completed

CompletedNCT01141504

Effect of Oral Adenosine-triphosphate (ATP) on Human Muscle Performance

Effect of Oral ATP on Human Muscle Performance

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Metabolic Technologies Inc. · Industry
Sex
All
Age
20 Years – 30 Years
Healthy volunteers
Accepted

Summary

Adenosine-triphosphate (ATP) serves as the sole energy source for muscle contraction. Therefore human performance of brief maximal exercise is limited, in part, by the availability of ATP to the contracting muscle. Because muscle ATP storage is small (enough to sustain maximal exercise for less than 1 second), factors that enhance either storage or resynthesis of ATP may have a positive impact on repeated muscle contractions. The current study will test the hypothesis that increasing ATP availability to muscle via oral supplementation will improve performance of repeated high intensity exercise as measured by a) work performed in each of the three 50 contraction fatigue tests, b) sum of total work performed, and c) percentage decrement in total work from the first to third third 50 contraction test.

Detailed description

To date we have studied 10 subjects who have followed through with all 3 of the original interventions (Placebo, 250 mg PeakATP/d and 400 mg PeakATP/d). Currently we have received approval and are expanding the study with 5 additional subjects who will receive the Placebo, 400 mg PeakATP/d and the 400 mg PealATP/d plus proprietary blend interventions.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPeakATP 250The nutritional intervention provides for oral ingestion of 250 mg PeakATP per day
DIETARY_SUPPLEMENTPlaceboPlacebo capsules that are comparable in size and color to the active comparator for blinding purposes
DIETARY_SUPPLEMENTPeakATP 400The nutritional intervention provides for oral ingestion of 400 mg PeakATP per day
DIETARY_SUPPLEMENTPeakATP 400 plus proprietary blendThe nutritional intervention provides for oral ingestion of 400 mg PeakATP per day plus a proprietary blend of additional nutrients

Timeline

Start date
2010-06-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2010-06-10
Last updated
2012-01-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01141504. Inclusion in this directory is not an endorsement.