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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02255630
Other study ID # H14-02788
Secondary ID
Status Completed
Phase N/A
First received September 16, 2014
Last updated November 9, 2016
Start date January 2015
Est. completion date August 2016

Study information

Verified date November 2016
Source University of British Columbia
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

Athletes using inhaled β2-adrenoreceptor agonists (IBAs) win a disproportionate number of medals. However, most previous research has shown that β2 agonists do not improve exercise performance in either asthmatic or non-asthmatic athletes. Although the majority of these studies do not show an ergogenic effect, the small number of studies with extended exercise bouts (~60 minutes) do show an advantage. The investigators believe that a controlled yet sport-specific exercise protocol will elucidate this ergogenic effect. Because IBAs may have different effects on these two groups of athletes, the investigators will measure exercise performance in both female and male elite cyclists. The investigators hypothesize that athletes will perform better during a combination steady-state/sprint exercise task following salbutamol administration.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date August 2016
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 19 Years to 40 Years
Eligibility Inclusion Criteria:

- maximal oxygen consumption of =60 and =55 mL·kg-1·min-1 or =5·L·min-1 and =4·L·min-1 for men and women

Exclusion Criteria:

- pregnant women

- any history of uncontrolled respiratory or cardiac disease

- smokers

- diabetics

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Cycling Exercise


Locations

Country Name City State
Canada University of British Columbia, Environmental Physiology Laboratory Vancouver British Columbia

Sponsors (2)

Lead Sponsor Collaborator
University of British Columbia Natural Sciences and Engineering Research Council, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Peak Power Output peak power output of the final 30 seconds of the cycling bout will be assessed. No