Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02454049
Other study ID # 2015-04
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2016
Est. completion date December 2018

Study information

Verified date January 2019
Source Swiss Paraplegic Centre Nottwil
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate wether beetroot juice or sodium nitrate enhances time trial performance in Swiss paracycling athletes compared to the ingestion of a placebo supplement. Furthermore, the effects of beetroot juice and sodium nitrate on performance will be investigated in spinal cord injured and non-injured athletes.


Description:

The influence of dietary nitrate on performance will be tested performing a time trial on a handbike. The time trial will be the same as in the Paralympics 2016 in Rio. The subjects perform three trials and receive another supplement for each trial: beetroot juice with 6mmol nitrate, 6mmol sodium nitrate or plain water (placebo supplement). The time to complete the time trial will be the main outcome parameter.


Recruitment information / eligibility

Status Completed
Enrollment 9
Est. completion date December 2018
Est. primary completion date November 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- healthy paracycling athletes

- healthy, able-bodied, upper-body trained individuals

Exclusion Criteria:

- female

- smoking

- any medication affecting performance

- medical conditions affecting performance

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
beetroot juice
6mmol nitrate
sodium nitrate
6mmol sodium nitrate
water
plain water

Locations

Country Name City State
Switzerland Swiss Paraplegic Centre Nottwil Lucerne

Sponsors (1)

Lead Sponsor Collaborator
Swiss Paraplegic Centre Nottwil

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary time to perform trial 3 hours after supplement ingestion
Secondary oxygen consumption during time trial performance measured by a metabolic cart (Oxycon Pro) in ml/min/kg 3 hours after supplement ingestion