Clinical Trials Directory

Trials / Completed

CompletedNCT01265355

Community Based Prevention of Rotavirus Gastroenteritis by a Functional Food Supplement

Community Based Prophylaxis for Rotavirus Gastroenteritis in Children by an Anti-rotavirus Protein Based Food Supplement

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
330 (actual)
Sponsor
Christian Medical College, Vellore, India · Academic / Other
Sex
All
Age
6 Months – 12 Months
Healthy volunteers
Accepted

Summary

Rotavirus is the commonest cause of severe gastroenteritis in young children worldwide. The investigators hypothesize that use of a food based prophylactic will decrease incidence of rotavirus infection in young children in south India, prevent intestinal damage and overall result in lower infection rates and better gut function. This trial will evaluate the efficacy of prevention of rotavirus gastroenteritis when an anti-rotavirus protein or antibody fragments expressed in yeast or placebo are given daily as a food supplement to children between the ages of 6 and 12 months. The children will followed for one year and rates of rotavirus diarrhoea, antibody responses and gut function will be compared between children receiving antibody fragments or placebo.

Detailed description

The study will be carried out in an urban slum area in Vellore, south India. Children between the ages of 6 and 12 months will be recruited for participation in the study. They will be randomized to receive supplementation with ARP or placebo, and will be followed for a period of one year, with weekly home visits and monitoring of all episodes of diarrhoea. In addition, every two weeks, surveillance stool samples will be collected and tested for rotavirus to identify asymptomatic infections by PCR. All episodes of diarrhoea will be investigated intensively for bacterial, viral and parasitic agents of diarrhoea using both conventional and molecular techniques and all cases will be treated appropriately at the study clinic or referral hospital as required. Monthly anthropometric measurements will be carried out to estimate rates of growth and to identify growth faltering. Blood samples will be taken at 4, 8 and 12 months for estimation of anti-rotavirus IgA and IgG antibodies. Studies on intestinal absorption and permeability will be carried out at recruitment, 6 and 12 months by the lactulose:mannitol test (measured by HPLC detection of sugars). All rotavirus strains obtained will be characterized by genotyping.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTAnti-rotavirus protein11mg ARP In 1 Gm Product Daily For 12 Months, given in orange juice
DIETARY_SUPPLEMENTMaltodextrinMaltodextrin 1 gm daily

Timeline

Start date
2011-03-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2010-12-23
Last updated
2015-02-04

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT01265355. Inclusion in this directory is not an endorsement.