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Evaluation of a Probiotic On Anxiety and Stress in Healthy Adults Sensible to Daily Stress

NCT00807157 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2009-04-24

No results posted yet for this study

Summary

The purpose of the the study is to determine if PROBIOSTICK® decrease stress and anxiety of people sensible to daily stress.

Conditions

Interventions

DIETARY_SUPPLEMENT

PROBIOSTICK® during 30 days

Every morning subjects will consume a stick of PROBIOSTICK® during 30 days

DIETARY_SUPPLEMENT

Placebo during 30 days

Every morning subjects will consume a stick of placebo during 30 days

Sponsors & Collaborators

  • Institut Rosell Lallemand

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2009-04-30
Completion
2009-04-30

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

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 NCT00807157 on ClinicalTrials.gov