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Ready to Use Therapeutic Food (RUTF) in Severe Malnourished Children (RUTF)

Primary Purpose

Severe Acute Malnutrition

Status
Completed
Phase
Not Applicable
Locations
Bangladesh
Study Type
Interventional
Intervention
Plumpy Nut
Khichuri and Halwa
Sponsored by
International Centre for Diarrhoeal Disease Research, Bangladesh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Severe Acute Malnutrition focused on measuring RUTF, Severe Acute Malnutrition, Children, Body composition, Microbiota, Short Chain Fatty Acid, Acceptability of RUTF, Edema free 15 percent weight gain, Changes in body composition, Gut microbiota, Genome wide association

Eligibility Criteria

6 Months - 24 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Children with SAM, defined as WH <- 3 Z score of WHO standard and/or bipedal nutritional oedema (according to WHO growth standard)
  2. Sex: Either
  3. Age: 6-24 months
  4. Completed acute (stabilization) phase management and regaining appetite
  5. No signs of concurrent infection (e.g. diarrhoea, lower respiratory tract infection/pneumonia, severe anaemia, fever, sepsis, electrolyte imbalance, etc.)
  6. Mothers/caregivers agreed to stay in the NRW until child achieve desired discharged criteria.
  7. Informed consent given by the parent or guardian.

Exclusion Criteria:

  1. Children without fixed residential address
  2. Children with tuberculosis or any congenital/acquired disorder
  3. Any physical condition that affects normal feeding of the children e.g. Cleft lip or palate.

Sites / Locations

  • International Centre for Diarrhoeal Diseases Research, Bangladesh

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

RUTF

Khichuri - Halwa

Arm Description

Ready to use Therapeutic Food (RUTF) Plumpy nut.

Cereal Legume

Outcomes

Primary Outcome Measures

Rate of weight gain
During stay in nutrition rehabilitation unit, Dhaka Hospital

Secondary Outcome Measures

Days require to achieve oedema free discharge criteria and other anthropometric changes
Weight for length -2 SD or 15 percent weight gain

Full Information

First Posted
April 6, 2011
Last Updated
July 26, 2015
Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
International Atomic Energy Agency, Washington University School of Medicine, University of Virginia
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1. Study Identification

Unique Protocol Identification Number
NCT01331044
Brief Title
Ready to Use Therapeutic Food (RUTF) in Severe Malnourished Children
Acronym
RUTF
Official Title
Efficacy and Acceptability of Ready to Use Therapeutic Food (RUTF) in Children Aged 6-24 Months With Severe Acute Malnutrition in Bangladesh
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
International Atomic Energy Agency, Washington University School of Medicine, University of Virginia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
RUTF would be more effective (quicker catch-up growth by promoting more tissue accrue resulting decrease stay in rehabilitation ward) in treating children with SAM during the rehabilitation phase than khichuri /halwa; RUTF would be acceptable to the children and their mothers/caregivers; Malnutrition is not caused solely by lack of food, but also by impaired utilization of the food that is ingested. The ability of the gut to absorb nutrients from the diet is associated with the host's 'human' genotype, the host's gut microbiota and its gene content (the microbiome).
Detailed Description
We propose to conduct a research study to compare the acceptability and efficacy of RUTF with that of the cereal-based diets in the management of hospitalised SAM children in Bangladesh. After completion of the initial acute phase treatment (for diarrhoea, lower respiratory tract infection/pneumonia, severe anaemia, fever, sepsis, electrolyte imbalance, and/or anorexia) in the Longer Stay Ward/ Special Care Ward of the Dhaka Hospital, the children will be transferred to the NRW according to the enrolment criteria. Once the children fulfil all the criteria for entry into the study and written consent to their participation is obtained from respective parents/guardian, they will be randomly allocated to: (i) the standard cereal-based foods, namely khichuri and halwa, or (ii) RUTF. Randomization will be done according to computer-generated random numbers using permuted blocks with block lengths of four and six. For understandable reasons, the dietary therapy can't be blinded. The assigned treatment packages will be kept in closed opaque envelopes until the same serial number is assigned to an enrolled child. Participating children will be discharged from NRW according to the new WHO growth standard (WHO, 2009), which explicit , at least after seven days stay completed there or until achieving a weight gain of 15% , for non-oedematous child. On the other hand for oedematous child after oedema free if WHZ is ≥-3; however if oedema free WHZ is <- 3 then the child will be discharge after achieving 15% weight gain. In both the groups, the acceptability of the allocated diet, both by the children and their respective mothers/caregivers, the rate of weight gain and anthropometric measurements, and adverse event will be systematically recorded for analyses. Khichuri/halwa group will be given diet as per standardized management protocol of NRW of the Dhaka Hospital. On the other hand, children allocated to RUTF will receive commercially available RUTF (Plumpy nut) in a total of 200 kcal/kg.day in a sequential manner (Plumpy nut will be offered ~ 125 kcal/kg in 1st 24 hours, ~ 150 kcal/kg in 2nd 24 hours, then~200k cal/kg by the third day). We will also examine if the weight gain of the children is associated with increase in the lean body mass or in the body fat mass by assessing their body composition, Changes in body composition after dietary intervention in SAM children will be assessed by non-invasive technique using stable isotope tracer (deuterium oxide). For this, after collection of baseline urine and saliva samples a known quantity (5 gm) of deuterium oxide labelled water will be given to all study children. Enrichment of deuterium in body water will be measured to estimate total body water (TBW). Enrichment reaches a plateau after 3-5 hours. According to the recommendation from International Atomic Energy Agency (IAEA) field manual, two post-dose saliva samples will be collected at 3rd and 4th hours. The concentrations of deuterium in saliva samples will be measured with Fourier Transform Infrared Spectrometer (FTIR). The urine specimens will be analyzed using Isotope Ratio Mass Spectrometry (IRMS). From measured TBW we would estimate the fat free mass (FFM). Body fat mass (FM) is the difference between body weight and fat free mass. This procedure will be repeated in same sequence in all study children at the end of dietary intervention when the study child achieve discharge criteria. In addition to the above mentioned procedures, anthropometric measures such as mid-arm circumference, triceps skin fold thickness, arm fat area and arm muscle area would also be routinely recorded along with other morbidity data. We wish to leverage the ongoing scientific collaboration among University of Virginia, Center for Genome Sciences at Washington University School of Medicine, USA and ICDDR,B to gain insight into the influence of human genetic polymorphisms and gut microbiome on malnutrition, in order to provide a foundation for new treatment and prevention programs on a population-wide basis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Acute Malnutrition
Keywords
RUTF, Severe Acute Malnutrition, Children, Body composition, Microbiota, Short Chain Fatty Acid, Acceptability of RUTF, Edema free 15 percent weight gain, Changes in body composition, Gut microbiota, Genome wide association

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
224 (Actual)

8. Arms, Groups, and Interventions

Arm Title
RUTF
Arm Type
Experimental
Arm Description
Ready to use Therapeutic Food (RUTF) Plumpy nut.
Arm Title
Khichuri - Halwa
Arm Type
Active Comparator
Arm Description
Cereal Legume
Intervention Type
Dietary Supplement
Intervention Name(s)
Plumpy Nut
Intervention Description
to RUTF will receive commercially available RUTF (Plumpy nut) in a total of 200 kcal/kg.day in a sequential manner (Plumpy nut will be offered ~ 125 kcal/kg in 1st 24 hours, ~ 150 kcal/kg in 2nd 24 hours, then~200k cal/kg by the third day).
Intervention Type
Dietary Supplement
Intervention Name(s)
Khichuri and Halwa
Intervention Description
Day 1: Milk suji, 10ml/kg/ feed for 11 feed & halwa 10gm/kg; 2 feed per day 125kcal/kg.day Day 2: Milk suji, 10ml/kg/ feed for 11 feed & halwa 10gm/kg; 2 feed per day & khichuri 10gm/kg; 2 feed per day 150kcal/kg.day Day 3: Milk suji 100, 10ml/kg/ feed for 11 feed & halwa 10gm/kg; 2 feed per day & khichuri 10gm/kg; 2 feed per day 175kcal/kg.day Day 4: Milk suji 100, 10ml/kg/ feed for 11 feed & halwa 10gm/kg; 3 feed per day & khichuri 10gm/kg; 3 feed per day 200kcal/kg.day Day 5 onward: Milk suji 100, 10ml/kg/ feed 6 hourly (4 feed per day) & halwa 20gm/kg; 3 feed per day & khichuri 20gm/kg; 3 feed per day 200kcal/kg.day
Primary Outcome Measure Information:
Title
Rate of weight gain
Description
During stay in nutrition rehabilitation unit, Dhaka Hospital
Time Frame
14 days
Secondary Outcome Measure Information:
Title
Days require to achieve oedema free discharge criteria and other anthropometric changes
Description
Weight for length -2 SD or 15 percent weight gain
Time Frame
14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
24 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Children with SAM, defined as WH <- 3 Z score of WHO standard and/or bipedal nutritional oedema (according to WHO growth standard) Sex: Either Age: 6-24 months Completed acute (stabilization) phase management and regaining appetite No signs of concurrent infection (e.g. diarrhoea, lower respiratory tract infection/pneumonia, severe anaemia, fever, sepsis, electrolyte imbalance, etc.) Mothers/caregivers agreed to stay in the NRW until child achieve desired discharged criteria. Informed consent given by the parent or guardian. Exclusion Criteria: Children without fixed residential address Children with tuberculosis or any congenital/acquired disorder Any physical condition that affects normal feeding of the children e.g. Cleft lip or palate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sayeeda Huq, MBBS, MIPH
Organizational Affiliation
International Centre for Diarrhoea Diseases Research, Bangladesh
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Centre for Diarrhoeal Diseases Research, Bangladesh
City
Dhaka
ZIP/Postal Code
1212
Country
Bangladesh

12. IPD Sharing Statement

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Ready to Use Therapeutic Food (RUTF) in Severe Malnourished Children

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