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Clinical Trials/NCT00534170
NCT00534170UnknownPhase 3

Randomized Controlled Field Trial of a Probiotics to Assess Its Role in The Prevention of Acute Diarrhoeal Diseases in Children

Indian Council of Medical Research1 site in 1 country4,000 target enrollmentStarted: June 1, 2007Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 3
Enrollment
4,000
Locations
1
Primary Endpoint
Diarrhoeal episodes in children

Study Overview

Brief Summary

A therapeutic as well as preventive role of probiotics has been suggested from results of different studies using different probiotics that have been tested, usually lactic acid producing bacteria such as lactobacillus, bifidobacterium and streptococcus species. The supplementation of probiotics to infants may also have a prophylactic effect against acute diarrhoeal diseases.

In the present proposal, we plan to examine if daily intake of a probiotic beverage, which includes 15 billion probiotic Lactobacilli, has a beneficial role in protecting children from infectious diarrhea in Kolkata.

OBJECTIVES

Primary objectives:

  1. To assess the impact of probiotics in the prevention of acute diarrhoeal diseases in children
  2. To assess the impact of probiotics on nutrition and growth of the children

Secondary Objectives:

  1. Reduction in duration, frequency of diarrhoea
  2. Identification of pathogens causing diarrhoea
  3. Examination of faecal microflora

STUDY DESIGN

It will be a double blind randomized controlled field trial involving 4000 children aged between 1 and 5 years in an urban slum of Kolkata, India. The 4000 children will be identified through demographic survey. The study will be double blinded where the study arm will receive Probiotic drink, which includes 15 billion probiotic Lactobacilli, one bottle (65ml) daily (under supervision of a Health Worker) for 12 weeks and the control arm will receive a similar drink without the lactobacilli (Nutrient drink) daily for 12 weeks. Randomization will be done in a ratio of 1:1, i.e., the study arm and control arm will include 2000 children each. All the children under the study will be visited daily by a health worker who will supervise intake of Probiotic drink or Nutrient drink by the children. All the children will be followed up daily for 24weeks for identification of acute diarrhoea cases.

Detailed Description

A therapeutic as well as preventive role of probiotics has been suggested from results of different studies using different probiotics that have been tested, usually lactic acid producing bacteria such as lactobacillus, bifidobacterium and streptococcus species. The supplementation of probiotics to infants may also have a prophylactic effect against acute diarrhoeal diseases.

In the present proposal, we plan to examine if daily intake of a probiotic beverage, which includes 15 billion probiotic Lactobacilli, has a beneficial role in protecting children from infectious diarrhea in Kolkata.

OBJECTIVES

Primary objectives:

  1. To assess the impact of probiotics in the prevention of acute diarrhoeal diseases in children
  2. To assess the impact of probiotics on nutrition and growth of the children

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
12 Months to 59 Months (Child)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Children of either sex aged 1-5 years will be eligible for screening and parents will give and a written, informed consent form will be required from either of the parents/ guardians of each participating child.
  • •Participating children should be free from any chronic illness and also any recent illness that may compromise the immune system. In general they will have good health without known underlying illness

Exclusion Criteria

  • •Children below -2SD of the National Center for Health Statistics (NCHS) reference median in the nutritional parameters will not be enrolled.
  • •Children with history of diarrhoea in the preceding 2 weeks will not be eligible.

Arms & Interventions

A,F,T,K

Experimental

Two arms are for intervention and two are for control or placebo

Intervention: Probiotic (Yakult) (Dietary Supplement)

Outcomes

Primary Outcomes

Diarrhoeal episodes in children

Time Frame: 10 months

Secondary Outcomes

  • nutritional status in children(10 months)

Investigators

Sponsor Class
Other Gov

Study Sites (1)

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