Effects of Lactobacillus Casei on Respiratory and Gastrointestinal Diseases in Adults
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ClinicalTrials.gov Identifier: NCT02541539 |
Recruitment Status :
Completed
First Posted : September 4, 2015
Last Update Posted : November 6, 2017
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Condition or disease | Intervention/treatment | Phase |
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Healthy Volunteers | Dietary Supplement: Lactobacillus casei Zhang Dietary Supplement: Placebo | Not Applicable |

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 |

Arm | Intervention/treatment |
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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.
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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.
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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. |
- 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
- 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
- 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

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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 |
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

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
Malaysia | |
School of Industrial Technology, Universiti Sains Malaysia | |
Pulau Pinang, Penang, Malaysia, 11800 |
Principal Investigator: | Min tze Liong, PhD | USM |
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 |