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OpenTrials
Completed

NCT Number: NCT03032549

Safety of a Ready to Drink Supplement

This study will examine a Ready to Drink (RTD) supplement.

Completed

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Key information

Conditions

Dietary Supplements

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This study will examine the short-term (7 days) characteristics of ingesting a Ready to Drink (RTD) supplement immediately prior to exercise on the blood, heart rate, blood pressure and self-reported side effects.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants are apparently healthy and recreationally active males and females between the ages of 18 and 40

Exclusion criteria

  • Participants are under 18 years old and above 40 years old
  • Participants have a history of treatment for metabolic disease (i.e., diabetes), hypertension, hypotension, thyroid disease, arrhythmias and/or cardiovascular disease
  • Participants currently use any prescription medication (birth control is allowed)
  • Participants are pregnant or lactating females or plan to become pregnant within the next month
  • Participants have a history of smoking
  • Participants drink excessively (12 drinks per week or more)
  • Participants have a recent history of creatine supplementation within 8 weeks of the start of supplementation

Treatment and study plan

RTD

Dietary Supplement

Ready to Drink Supplement

Placebo

Dietary Supplement

Placebo

Primary outcomes

  1. The effects of ingesting an RTD immediately prior to exercise on the blood

    Time frame: 7 days

  2. The effects of ingesting an RTD immediately prior to exercise on heart rate

    Time frame: 7 days

  3. The effects of ingesting an RTD immediately prior to exercise on blood pressure

    Time frame: 7 days

Secondary outcomes

  1. The effects of ingesting an RTD immediately prior to exercise on self-reported side effects

    Time frame: 7 days

Sponsors and collaborators

Lead sponsor

Texas A&M University

Other

Registry information

Official study title

Short-Term Safety and Dose Effects of a Ready to Drink Pre-Workout Supplement

Acronym: NB10

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Jan 26, 2017
Registry last updated
Jan 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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