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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03655041
Other study ID # 24WKBA
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2013
Est. completion date December 15, 2017

Study information

Verified date August 2018
Source University of Sao Paulo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Although β-alanine (BA) has been shown to be an effective ergogenic aid, little information exists on the safety of chronic supplementation despite potential concerns. The aim of this study was to investigate the effects of chronic BA supplementation on muscle taurine content, blood clinical markers and sensory side-effects during 24 weeks of BA supplementation.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date December 15, 2017
Est. primary completion date December 15, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy males

Exclusion Criteria:

- Smokers

- Chronic disease

- Prior or current use of steroids

- Use of creatine in the last 6 months

- Use of beta-alanine in the last 6 months

Study Design


Related Conditions & MeSH terms

  • Sports Nutritional Physiological Phenomena

Intervention

Dietary Supplement:
Beta-alanine
Beta-alanine in sustained-release tablets to increase muscle carnosine content
Placebo
Maltodextrin is used as a placebo as it does not lead to any increases in muscle carnosine

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Sao Paulo

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle taurine content in mmol/kg Change in the content of taurine in muscle will be determined using High-Pressure Liquid Chromatography of muscle biopsies Up to 24 weeks
Secondary Aspartate transaminase; alanine aminotransferase; alkaline phosphatase; lactate dehydrogenase and creatine kinase in U/L Aspartate transaminase; alanine aminotransferase; alkaline phosphatase; lactate dehydrogenase and creatine kinase will be analysed from venous blood samples Up to 24 weeks
Secondary Albumin; globulin; creatinine in mg/dL Albumin; globulin; creatinine will be analysed from venous blood samples Up to 24 weeks
See also
  Status Clinical Trial Phase
Completed NCT02474628 - Consistencies in Responses to Sodium Bicarbonate? N/A
Not yet recruiting NCT03505970 - Blood, Muscle and Exercise Responses to Sodium Bicarbonate Supplementation N/A