Safety of a Ready to Drink Supplement

NCT03032549 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2017-01-26

No results posted yet for this study

Summary

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

Conditions

  • Dietary Supplements

Interventions

DIETARY_SUPPLEMENT

RTD

Ready to Drink Supplement

DIETARY_SUPPLEMENT

Placebo

Placebo

Sponsors & Collaborators

Principal Investigators

  • Richard B Kreider, PhD · Texas A&M University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-01
Primary Completion
2016-09-01
Completion
2016-09-01

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03032549 on ClinicalTrials.gov