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NCT03501238 · ClinicalTrials.gov registry record · NA

Interaction of Salivary Proteins and Polyphenols

A NA study of Diet Habit and Diet Modification, sponsored by Purdue University.

Completed
Registry status
NA
Development phase
63
Enrollment target
1
Study location

NCT03501238 is a NA study of Diet Habit and Diet Modification that has completed, run by Purdue University. The registered enrollment target is 63 participants, below the 11,773-participant average among 22 other Diet Habit trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03501238, a NA study of Diet Habit and Diet Modification, has completed, sponsored by Purdue University.

COMPLETED
Registry status
NA
Development phase
63 participants
Enrollment target
1
Study location

Study Summary

Participants will be chosen through an initial sensory test to find high and low-perceivers of astringency. Selected participants will drink a chocolate milk or milk substitute beverage for one week each with washout weeks in between. At the end of each week participants will taste and rate multiple beverages for their astringency and other sensory properties. Participants will provide saliva samples weekly for proteomic analysis and (potentially) analysis of polyphenols. Participants will also be asked to provide a 24 hour dietary recall once per week. Data will be analyzed to determine if there is a relationship between polyphenol exposure, astringency ratings, and salivary protein composition.

Interventions

  • OTHER Chocolate Milk
  • OTHER Chocolate milk substitute
  • OTHER Chocolate milk substitute with gelatin

Study Locations (1)

Indiana

  • Purdue University - West Lafayette

Trial Details

FieldValue
Enrollment Target 63 participants
Start Date 2017-06-08
Est. Completion 2018-01-01
Phase NA

Sponsor

Purdue University

141 total trials

What the Registry Record Tells You About NCT03501238

The ClinicalTrials.gov registry entry for NCT03501238 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 63 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 11,773-participant average among 22 other Diet Habit trials with a reported enrollment target (99% lower). The listed sponsor is Purdue University, which has 141 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Diet Habit appearing as the primary indexed condition, and to 3 interventions - of which Chocolate Milk is the first listed.

NCT03501238 reports 1 study location spanning 1 distinct geographic area - top geographies include Indiana.

Frequently Asked Questions

What is clinical trial NCT03501238 about?

NCT03501238 is a clinical study titled "Interaction of Salivary Proteins and Polyphenols". Participants will be chosen through an initial sensory test to find high and low-perceivers of astringency. Selected participants will drink a chocolate milk or milk substitute beverage for one week each with washout weeks in between. At the end of each week participants will taste and rate multiple...

What is the current status of trial NCT03501238?

This trial is currently completed. It is a NA study. The enrollment target is 63 participants. The study started on 2017-06-08. Estimated completion is 2018-01-01.

What conditions does trial NCT03501238 study?

This clinical trial studies the following conditions: Diet Habit, Diet Modification, Taste, Altered, Saliva Altered.

What interventions are being tested in trial NCT03501238?

The interventions under investigation include: Chocolate Milk (OTHER), Chocolate milk substitute (OTHER), Chocolate milk substitute with gelatin (OTHER).

Who is sponsoring clinical trial NCT03501238?

This trial is sponsored by Purdue University, which has 141 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03501238 being conducted?

This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.