NCT00813553

Brief Summary

Carnosine is a natural acid buffering substance of muscle. The primary objective of this study is to test whether a nutritional supplement of beta-alanine enhances carnosine content in muscle.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Dec 2008

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2008

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

December 22, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 23, 2008

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2009

Completed
Last Updated

April 25, 2012

Status Verified

April 1, 2012

Enrollment Period

10 months

First QC Date

December 22, 2008

Last Update Submit

April 24, 2012

Conditions

Keywords

physical fitnessexerciseamino acid

Outcome Measures

Primary Outcomes (1)

  • muscle carnosine concentration

    0 to 8 weeks

Study Arms (3)

beta-alanine 0

PLACEBO COMPARATOR
Dietary Supplement: placebo

beta-alanine 1

EXPERIMENTAL
Dietary Supplement: beta-alanine

beta-alanine 2

EXPERIMENTAL
Dietary Supplement: beta-alanine

Interventions

placeboDIETARY_SUPPLEMENT

daily

beta-alanine 0
beta-alanineDIETARY_SUPPLEMENT

daily

beta-alanine 1

Eligibility Criteria

Age18 Years - 40 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Stable health as evaluated by medical evaluation
  • Body mass index higher than 18 kg/m2
  • Body mass index lower than 25 kg/m2, unless body fat is less than 20%

You may not qualify if:

  • intolerance to β-alanine,
  • allergy to soy, fish and crustacean
  • participation in another intervention study
  • consumer of dietary supplement susceptible to contain beta-alanine
  • determined to have very high baseline muscle carnosine concentration

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University and Inselspital

Bern, Canton of Bern, 3010, Switzerland

Location

MeSH Terms

Conditions

Motor Activity

Interventions

beta-Alanine

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

AlanineAmino AcidsAmino Acids, Peptides, and Proteins

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Intervention Model
PARALLEL
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 22, 2008

First Posted

December 23, 2008

Study Start

December 1, 2008

Primary Completion

October 1, 2009

Study Completion

October 1, 2009

Last Updated

April 25, 2012

Record last verified: 2012-04

Locations