Antibacterial Treatment Against Diarrhea in Oral Rehydration Solution

Diarrhea Clinical Trial

Official title:

Randomized, Double Blind Placebo-controlled Studies to Evaluate the Effect of an Orally-fed Escherichia Coli (E. Coli) Phage in the Management of ETEC and EPEC Induced Diarrhea in Children

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00937274
• Other study ID #: 08.11.INF
• Status: Terminated
• Phase: N/A
• First received: July 8, 2009
• Last updated: November 12, 2013
• Start date: August 2009
• Est. completion date: January 2013

Study information

• Verified date: November 2013
• Source: Nestlé
• Contact: n/a
• Is FDA regulated: No
• Health authority: Bangladesh: Bangladesh Medical Research CouncilBangladesh: Ethical Review Committee
• Study type: Interventional

Clinical Trial Summary

This study hopes to demonstrate the potentials of a new form of therapy for childhood diarrhea, a major cause of morbidity and deaths in Bangladesh and other developing countries, and thus a priority for improving child health.

Description:

This randomized double-blind, placebo controlled trial (RCT) aims to evaluate the effect of oral administered E. coli phage in children aged 4-60 months of age with proven ETEC and EPEC diarrhea. Children will be screened to exclude V. cholerae infections by dark field microscopy, rotavirus by stool ELISA, and invasive diarrhoea clinically as well as by stool microscopy, to identify children with possible ETEC and EPEC diarrhoea. Enrolled children will be randomly assigned, in equal numbers, to receive either: (i) a new T4 phage cocktail or (ii) Russian anti-E. coli phage cocktail (Microgen) at the dose recommended by the manufacturer or (iii) only oral rehydration solution (placebo) for 5 days in addition to management of dehydration and continued feeding in accordance with WHO guidelines. Duration of diarrhea, daily and cumulative stool output, volume of oral rehydration solution intake, stool frequency, time to recovery and weight gain will be the main outcome measures. As the dose of phage we intend to use in this therapeutic trial is higher than the dose administered to young children in earlier safety trial, we plan to initially conduct a safety study with these three study products in 45 children with non cholera, non rotavirus and non invasive diarrhea, to randomize equally in the three intervention groups, as for the final study mentioned above. The outcome measures in this safety part will include assessment of laboratory parameters including renal and liver function tests, haematological indices, and microbiological efficacy of phage by measuring phage and E. coli titre in daily stool samples. If the higher dose is found safe, tolerable, and not associated with any significant adverse event, we will proceed to the clinical efficacy trial.

We believe if T4 coli phage is assessed to be effective in the overall diarrhea management, this might lead to development of an affordable and sustainable adjunct to the currently available case management of E. coli diarrhea, benefiting millions of children worldwide.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 120
• Est. completion date: January 2013
• Est. primary completion date: January 2013
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 6 Months to 24 Months

Eligibility

Inclusion Criteria:

1. Sex: male

2. Age: 6 - 24 months

3. Better nourished (weight for age > 60 NCHS median)

4. H/o. diarrhea of less than 48 hours

5. Written informed consent from either parents/guardian (thumb impression for those who are not literate) for children

6. Negative test results for dark field microscopy of Vibrio cholerae and ELISA test for rotavirus in initial stool samples

Exclusion Criteria:

1. Systemic infection requiring antibiotic treatment

2. Severe malnutrition (W/A < 60%)

3. Unwilling to comply with study procedures

4. Currently participating or have participated in another clinical trial within the last 4 weeks at screening

5. Clinically significant abnormalities from medical history, physical examination, vital signs, haematology, clinical chemistry results, or other laboratory abnormalities

6. Clinically suggestive of invasive diarrhea

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Diarrhea

Intervention

Other:
• T4 phage cocktail test
T4 phages 106 PFU/ ml up to 5 days
• Commercial T4 phage cocktail
Treatment as recommended by the manufacturer (Microgen phages)
• standard oral rehydration solution (ORS)
Standard hospital treatment with ORS

Locations

Country	Name	City	State
Bangladesh	Clinical Sciences Division, ICDDR,B, Mohakhali,	Dhaka

Sponsors (1)

Lead Sponsor	Collaborator
Nestlé

Country where clinical trial is conducted

Bangladesh, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assessment of safety, tolerability and efficacy (reduce severity of diarrhea assessed by reduced stool volume and stool frequency) of oral administration of T4 phages in young children with diarrhea due to ETEC and/or EPEC infections		5 days	Yes
Secondary	Clinical assessment, blood tests, morbidity, duration of hospitalization		5 days	Yes