ClinicalTrials.Veeva

Menu

Effectiveness of Nutritional Products to Treat Moderate Acute Malnutrition

C

Centre for Food and Nutrition Research, Yaounde

Status and phase

Completed
Phase 2

Conditions

Wasting
Moderate Acute Malnutrition

Treatments

Dietary Supplement: A daily ration of 40 kcal/kg of body weight during 56 days

Study type

Interventional

Funder types

Other

Identifiers

NCT01898871
CMR6010

Details and patient eligibility

About

The purpose of this study is to determine whether an improved corn-soya blend (CSB+) and a new formulated ready-to-use supplementary food (RUSF) are effective in the treatment of moderate acute malnutrition in children.

Full description

Assuming the availability of some food in the household, the caregivers were instructed on how best to use the food they have and the quantity of supplementary food distributed was calculated to provide about 50% of child energy requirement.

Enrollment

81 patients

Sex

All

Ages

6 to 59 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children aged 6-59 month
  • Weight-for-height between -3 and -2 z-scores without edema
  • Good appetite
  • Stable clinical conditions

Exclusion criteria

  • Weight-for-Height Z-score < -3
  • Presence of bilateral pitting edema
  • Unstable clinical conditions
  • Not showing appetite

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

81 participants in 2 patient groups

Ready to Use Suplementary Food (RUSF)
Experimental group
Description:
A daily ration of 40 kcal/kg of body weight during 56 days
Treatment:
Dietary Supplement: A daily ration of 40 kcal/kg of body weight during 56 days
Corn Soya Blend (CSB+)
Active Comparator group
Description:
A daily ration of 40 kcal/kg of body weight during 56 days
Treatment:
Dietary Supplement: A daily ration of 40 kcal/kg of body weight during 56 days

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems