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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01745016
Other study ID # 12-1787
Secondary ID
Status Completed
Phase N/A
First received December 5, 2012
Last updated April 29, 2013
Start date January 2013
Est. completion date April 2013

Study information

Verified date April 2013
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Beta-alanine, as a method to increase muscle carnosine, has been shown to enhance muscle buffering capacity and delay fatigue. Various fatigue tests have been utilized to examine the effectiveness of beta-alanine supplementation. The physical working capacity test has been used to show significant increases in physical working capacities following supplementation. The physical working capacity tests were originally developed by Moritani et al. 1981 and Devries et al. 1982 to measure the point of onset of muscular fatigue. It is hypothesized that beta-alanine will increase physical working capacity at heart rate threshold, thereby signifying a delay in fatigue.


Description:

An equal number of men and women will be recruited [Men, n=20 (10 placebo [PL]; 10 beta-alanine (Active)]; [Women,n=20 (10 PL; 10 Active)]. Men and women will be randomly assigned to respective groups to allow for equal numbers in supplement and placebo groups.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date April 2013
Est. primary completion date April 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

- Between the ages of 18-35 years old

- Be recreationally active (defined as accumulating 1-5 hours of moderate intensity

Exclusion Criteria

- Any health risks or indicators that would prevent them from participating in physical activity, as determined by a health history questionnaire

- Must not have taken performance enhancing supplements containing beta-alanine or creatine during the last 3 months

Study Design

Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Investigator)


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Placebo

Beta-alanine


Locations

Country Name City State
United States UNC Exercise and Sport Science Chapel Hill North Carolina

Sponsors (1)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Physical working capacity at heart rate threshold 0 to 4 weeks No
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