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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05354999
Other study ID # COCKTAIL
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date April 18, 2022
Est. completion date December 2023

Study information

Verified date August 2022
Source University of Copenhagen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to investigate the effect of combinations of creatine monohydrate, sodium bicarbonate and caffeine on exercise performance and fatigability.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 23
Est. completion date December 2023
Est. primary completion date March 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Healthy - VO2max of >50 ml/min/kg for men and >45 ml/min/kg for women - Performs endurance training >3 times per week Exclusion Criteria: - Chronic disease deemed by the study responsible medical doctor to interfere with any part of the study - Smoking - Chronic use of prescription medicine deemed by the study responsible medical doctor to interfere with any part of the study

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Sodium bicarbonate and caffeine
On experimental days subjects ingest a combination of sodium bicarbonate, caffeine and placebo.

Locations

Country Name City State
Denmark August Krogh Building Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Morten Hostrup, PhD

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Work performed (kJ/Watt) Work performed during a 6 minute time trial Measured at each trial throughout the study, on average 4 weeks
Secondary Work performed (kJ/Watt) Work performed during a 15 second sprint test Measured at each trial throughout the study, on average 4 weeks
Secondary Muscle strength (Nm) Maximal voluntary isometric contraction of m. quadriceps femoris Measured at each trial throughout the study, on average 4 weeks
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