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Effects of Lactobacillus Casei on Respiratory and Gastrointestinal Diseases in Adults

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02541539
Recruitment Status : Completed
First Posted : September 4, 2015
Last Update Posted : November 6, 2017
Sponsor:
Collaborator:
Inner Mongolia Agricultural University
Information provided by (Responsible Party):
Min-Tze LIONG, Universiti Sains Malaysia

Brief Summary:
This project aims to study the benefits of probiotics namely Lactobacillus casei Zhang (LCZ) in prevention of upper respiratory and gastrointestinal illnesses, which are found common among adults in Malaysia aged from 18 to 81 years.

Condition or disease Intervention/treatment Phase
Healthy Volunteers Dietary Supplement: Lactobacillus casei Zhang Dietary Supplement: Placebo Not Applicable

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 150 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Prevention
Official Title: Effects of Lactobacillus Casei in the Prevention of Upper Respiratory and Diarrheal Diseases Among Adults
Actual Study Start Date : October 1, 2015
Actual Primary Completion Date : September 30, 2016
Actual Study Completion Date : September 30, 2016

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: Lactobacillus casei Zhang
Intervention consists of daily administration of 2g probiotic Lactobacillus casei Zhang, administered daily at a fixed dosage of 9 log CFU/sachet/day and continue for 12 months.
Dietary Supplement: Lactobacillus casei Zhang
This project aims to study the benefits of probiotics namely Lactobacillus casei Zhang in prevention of upper respiratory and gastrointestinal illnesses, among adults in Malaysia aged from 18-81 years.
Other Name: LCZ

Placebo Comparator: Placebo
Intervention consists of daily administration of 2g placebo (no probiotic bacteria), administered daily and continue for 12 months.
Dietary Supplement: Placebo
This project aims to study the benefits of probiotics namely Lactobacillus casei Zhang in prevention of upper respiratory and gastrointestinal illnesses, among adults in Malaysia aged from 18-81 years.




Primary Outcome Measures :
  1. Serum immunoglobulin-A (IgA) level [ Time Frame: 12 months ]
    IgA as an indicator for immunology, in assessing severity of upper respiratory illnesses between number of adult participants taking LCZ vs. placebo

  2. Bristol stool chart scale [ Time Frame: 12 months ]
    Bristol stool scale (from a scale of 1-7; scale of 1 representing hard lump, and 7 representing liquid with no solid pieces) as an indicator for assessing severity of gastrointestinal-related diarrheal illnesses between number of adult participants taking LCZ vs. placebo


Secondary Outcome Measures :
  1. Fecal microbiota profiling [ Time Frame: 12 months ]
    Deoxyribonucleic acid (DNA) sequencing of fecal samples to compare DNA sequences of the different microbiota between adult participants taking LCZ vs. placebo



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 81 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Male/ female subjects
  • 18-81 years old
  • Body mass index (BMI) within a healthy range
  • Willing to commit throughout the experiment

Exclusion Criteria:

  • Type-1 diabetes
  • Long term medication due to certain severe illness
  • Human immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS)
  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency
  • Vegetarian

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02541539


Locations
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Malaysia
School of Industrial Technology, Universiti Sains Malaysia
Pulau Pinang, Penang, Malaysia, 11800
Sponsors and Collaborators
Universiti Sains Malaysia
Inner Mongolia Agricultural University
Investigators
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Principal Investigator: Min tze Liong, PhD USM
Publications of Results:
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Responsible Party: Min-Tze LIONG, Associate Professor Dr, Universiti Sains Malaysia
ClinicalTrials.gov Identifier: NCT02541539    
Other Study ID Numbers: 15020059
First Posted: September 4, 2015    Key Record Dates
Last Update Posted: November 6, 2017
Last Verified: November 2017