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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01418898
Other study ID # PEP 1011
Secondary ID
Status Recruiting
Phase Phase 4
First received August 15, 2011
Last updated August 16, 2011
Start date August 2011
Est. completion date April 2012

Study information

Verified date August 2011
Source PepsiCo Global R&D
Contact Imelda Angeles-Agdeppa, PhD
Phone 011-63-2-8372071
Email imelda_agdeppa@yahoo.com
Is FDA regulated No
Health authority Philippines: Ethics Committee
Study type Interventional

Clinical Trial Summary

This study will follow a randomized, double-blind, placebo-controlled, parallel-group design to test if an oat beverage fortified with iron, zinc vitamin A and vitamin C will improve nutrient status and iron deficiency in young children compared to an unfortified control beverage.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date April 2012
Est. primary completion date December 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 5 Years to 7 Years
Eligibility Inclusion Criteria:

- 5-7 years old

- Children with parental consent

- Not suffering from diarrhea, respiratory infections and fever at time of interview and for the past two weeks

- No history of blood disorder or malaria

- Had not participated in any feeding program for the past 4 months

- Children with Hb > 70 g/L to <120 g/L (WHO/UNICEF/UNU, 1998)

- CRP <10 mg/L

Exclusion Criteria:

- All children aged < 5 years old and > 7 years old

- Without parental consent

- Undergoing treatment for any chronic ailment, diagnosed as suffering from any sort of illness e.g. fever, diarrhea, stomach ache, cough and colds at the time of examination or during the past two weeks.

- Reported current or history of blood abnormalities/hemoglobinopathies

- Children with all normal Hb levels or very low Hb < 70 g/L

- CRP >10mg/L

Study Design

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


Intervention

Other:
Dietary Intervention
Nutrient fortified oat beverage

Locations

Country Name City State
Philippines FNRI Taguig City

Sponsors (2)

Lead Sponsor Collaborator
PepsiCo Global R&D PepsiCo - Philippines

Country where clinical trial is conducted

Philippines, 

Outcome

Type Measure Description Time frame Safety issue
Primary Iron status: Change in hemoglobin and serum ferritin Baseline and 4 months No
Secondary zinc, vitamin A and vitamin C status Baseline and 4 months No
Secondary Weight, height, CRP and frequency of illness Baseline and 4 months No
Secondary Dietary intake Baseline and 4 months No
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