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Clinical Study of Novel Probiotic Microbial Composite™ to Treat Undernourished Young Children

B

Biowish Technologies

Status

Unknown

Conditions

Malnutrition
Quality of Life
Growth Arrest

Treatments

Dietary Supplement: Probiotic Microbial Composite
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT03150927
BWT-20150720-001

Details and patient eligibility

About

This study is to determine if a novel bio-fermented Microbiotic Composite™ can improve the digestive health and subsequent growth and quality of life parameters in a selected group of children in a district in India.

Full description

The Probiotic Microbial Composite™ is a multifaceted technology that encompasses three key areas, namely, prebiotics, probiotics and post-biotics. The first component, prebiotics, involve non-digestible food ingredients, typically oligosaccharides which act by beneficially affecting the host by stimulating growth, activity, or in fact both of specific intestinal bacteria.

The probiotic component refers to the augmentation or addition of bacteria to enhance and support the various beneficial bacteria that are inherent to the gastrointestinal tract. The bio-fermented Microbiotic Composite™ is a consortium of bacteria which can play a significant physiological role as a probiotic. This theory, termed the microbial consortium theory suggests that rather than a cumulative effect by the bacteria, there is in fact combinatorial affect by the use of several species.

The final component post-biotics, in general, mimic the beneficial health promoting effects of probiotics whilst avoiding the risk of taking live micro-organisms within the gastrointestinal tract, especially in populations such as infants and the elderly in whom the intestinal barriers, as well as, innate immune defenses can be impaired. The term typically encompasses a vast plethora of byproducts, know as metabolites, produced and secreted by the bacteria in response to their environment.

Enrollment

250 estimated patients

Sex

All

Ages

3 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

The Randomized Clinical Trial (RCT) will typically involve 250 subjects randomized into two arms based on age and sex.

Following a positive outcome in the RCT (following 6 months), we envisage converting the study to an observational based study (case-study) based on ethical principles where the placebo arm of the study would be administered the test product. Each subject will be assessed for a total of two years.

Inclusion criteria:

  • Inpatient setting: Children with age of 3 years to 12 years with acute diarrhea
  • Outpatient setting: healthy children aged 3 years to 12 years

Exclusion criteria:

  • Subjects taking any kind of prescription medication.

  • Subjects taking any dietary supplements (2-week washout is permitted).

  • Subjects taking any antibiotics (must have discontinued antibiotic use 12-weeks prior to beginning study). An allowance will be made to existing subjects already taking part in the study. This confounder will however have to be noted by the primary investigators.

  • Individual has a condition the Investigator believes would interfere with his or her ability to provide informed consent, comply with the study protocol, which might confound the interpretation of the study results or put the person at undue risk.

    • Including subjects who are bed or wheelchair-bound
    • Including subjects who have any physical disability which could interfere with their ability to perform the functional performance measures included in this protocol.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

250 participants in 2 patient groups, including a placebo group

Probiotic Microbial Composite
Experimental group
Description:
Probiotic Microbial Composite is a safe, 100% natural material containing all Generally Recognized as Safe (GRAS) Probiotics, combined with FDA approved food grade excipient materials. The probiotics contained within are also all 100% natural and non-Genetically Modified Organisms (non-GMO).
Treatment:
Dietary Supplement: Probiotic Microbial Composite
Placebo
Placebo Comparator group
Description:
Placebo is a mixture of inactive ingredients found in Probiotic Microbial Composite. These ingredients are FDA approved food grade materials, 100% natural and palatable.
Treatment:
Dietary Supplement: Placebo

Trial contacts and locations

1

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Central trial contact

JoElla Barnes; Richard S Carpenter

Data sourced from clinicaltrials.gov

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