Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03495063

Synthetic and Natural Caffeine on Hemodynamic Parameters in Young, Healthy Volunteers

Comparison of Synthetic and Natural Caffeine on Hemodynamic Parameters in Young, Healthy Volunteers: A Randomized, Double Blind, Crossover Study

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
David Grant U.S. Air Force Medical Center · Federal
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study determine the difference in hemodynamic effects of synthetic and natural caffeine consumption in healthy individuals through blood pressure (central and peripheral) assessment. Participants will randomly be assigned to consume either one 8oz cup of coffee containing 400mg of caffeine (increased caffeine using concentrated coffee) or one 8oz cup of coffee-flavored drink with approximately 400mg synthetic caffeine from capsules dissolved in it.

Detailed description

The purpose of this study is to assess the difference in effects of consuming synthetic versus natural caffeine on hemodynamic parameters in healthy subjects. This study will determine the difference in hemodynamic effects of synthetic and natural caffeine consumption in healthy individuals through blood pressure (central and peripheral) assessment. The participants in this study are healthy adults who will be introduced to a risk that may be more than they would encounter through their normal daily activities. This study seeks to add to the literature by evaluating the difference in impact of synthetic compared to natural caffeine on central blood pressure. This protocol has the following aims: 1. Investigators hypothesize there will be a (baseline adjusted \[ΔBP\]) difference in BP (peripheral and central) between the natural and synthetic caffeine arms in healthy volunteers post consumption. 2. Investigators hypothesize there will be (baseline adjusted \[ΔCO\]) no difference in CO between the natural and synthetic caffeine arms in healthy volunteers post consumption. 3. Investigators hypothesize there will be (baseline adjusted \[ΔSVR\]) no difference in SVR between the natural and synthetic caffeine arms in healthy volunteers hours post consumption.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTNatural CaffeineConsumption of 400mg of natural caffeine
DIETARY_SUPPLEMENTSynthetic CaffeineConsumption of 400mg of synthetic caffeine

Timeline

Start date
2019-09-16
Primary completion
2020-11-01
Completion
2020-12-01
First posted
2018-04-11
Last updated
2020-04-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03495063. Inclusion in this directory is not an endorsement.