Efficacy of an Oral, Killed Enterotoxigenic Escherichia Coli Vaccine in Prevention of Diarrhea in Egyptian Infants and Young Children

Last updated: October 7, 2015
Sponsor: U.S. Army Medical Research and Development Command
Overall Status: Completed

Phase

3

Condition

Hyponatremia

Lactose Intolerance

Bowel Dysfunction

Treatment

N/A

Clinical Study ID

NCT02556996
HSRRB A-7965
  • Ages 6-18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

This is a randomized, double-blind, placebo-controlled clinical trial performed in Egyptian children 6-18 months of age. The primary aim of the study is to determine the protective efficacy of an oral, inactivated whole-cell enterotoxigenic Escherichia coli (ETEC) vaccine against diarrhea associated with excretion of ETEC that express a vaccine-shared antigen over a one year period of follow-up by active surveillance. The vaccine consists of a mixture of five formalin-killed ETEC bacteria expressing prevalent ETEC colonization factors and recombinant cholera toxin B-subunit (killed ETEC/rCTB vaccine). The placebo preparation is heat-killed Escherichia coli K-12 bacteria.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Willingness of parent to have the child participate;

  2. Plans to reside in catchment area continuously for at least one year

Exclusion

Exclusion Criteria:

  1. Global developmental delay

  2. Severe malnutrition

  3. Chronic bedridden status

  4. Serious chronic disorder requiring chronic medication

Study Design

Total Participants: 356
Study Start date:
October 01, 1998
Estimated Completion Date:
April 30, 2002