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Study of Psyllium 6.8 g Versus Placebo on Satiety in Healthy Volunteers

NCT01809925 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2014-10-28

No results posted yet for this study

Summary

This is a randomized, double-blind, placebo-controlled, 2-treatment, 3-period crossover design study to evaluate the effects of psyllium 6.8 g provided as sugarfree Metamucil fiber supplement powder dissolved in water versus placebo on satiety measures in healthy volunteers. This study will be conducted at a single study site.

Conditions

  • Hunger

Interventions

DIETARY_SUPPLEMENT

psyllium fiber 6.8g

Subjects will drink their assigned test product as quickly as possible immediately before eating breakfast at each visit.

DIETARY_SUPPLEMENT

placebo

Subjects will drink their assigned test product as quickly as possible immediately before eating breakfast at each visit.

Sponsors & Collaborators

  • Procter and Gamble

    lead INDUSTRY

Principal Investigators

  • Jose Brum, MD · Procter and Gamble

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2013-03-31
Primary Completion
2013-04-30
Completion
2013-04-30

Countries

  • United States

Study Locations

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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 NCT01809925 on ClinicalTrials.gov