Severe Acute Malnutrition Clinical Trial
Official title:
Efficacy of Ready to Use Therapeutic Food Using Soy Protein Isolate in Under-5 Children With Severe Acute Malnutrition in Bangladesh
Verified date | June 2016 |
Source | International Centre for Diarrhoeal Disease Research, Bangladesh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
SAM defined by having weight-for-height (WH) less than - 3 Z score or bi-pedal nutritional
edema is an important cause of death in children globally including Bangladesh. The death
rate among children hospitalized for SAM is still high. Severe malnutrition in children can
be successfully treated by using WHO guidelines with or without minor modification. Since the
Community Based Therapeutic Care (CTC)/CMAM approach was developed, the use of RUTF for the
treatment of children with SAM has gained ground, and huge amounts of RUTF are used
particularly in African countries. RUTFs are an energy-dense lipid paste enriched with
vitamins and minerals. The typical composition (ingredient % of weight) of RUTF is whole milk
powder 30%; sugar 28%; vegetable oil 15.4%; peanut paste 25%; and mineral vitamin mix 1.6%.
Although the CTC model promises treatment of SAM at a considerably lower cost than the
previous inpatient model, the cost of RUTF is still considered a significant barrier to
universal roll-out of SAM treatment and has made CTC implementation too expensive in many
high-need countries.
The single most expensive raw ingredient in RUTF is milk powder, contributing around 50% of
raw ingredient cost or between 30-35% of the total cost of the final product. Isolated soy
protein has a cost per kg protein that normally is below that of skim or whole milk powder,
and can thus reduce the total cost of RUTF. In addition, isolated soy protein (ISP) is a high
quality, complete protein that meets the daily protein requirements of growing children and
adults. ISP is a highly digestible protein [FAO/WHO, 1991] with an amino acid profile that
has been shown to achieve a Protein Digestibility-Corrected Amino Acid Score (PDCAAS) of
1.00, comparable to milk and eggs, and has been shown to maintain nitrogen balance when fed
as the sole protein source at minimum recommended intake levels.
To compare the efficacy (weight gain, rate of weight gain and change of lean body mass) of
the standard RUTF and an RUTF made from ISP (Soy-RUTF) through a randomized double masked
intervention trial 300 SAM children aged 6 to 59 months after completion of their
stabilization phase from the Dhaka Hospital of icddr,b Bangladesh will be studied. They will
randomly receive standard- or Soy-RUTF as take home and followed up (weekly until achieving
-2 WHZ, and thereafter fortnightly until achieving -1 WHZ) at the nutrition follow up unit at
the outpatient department of this Dhaka Hospital of icddr,b.
Status | Completed |
Enrollment | 260 |
Est. completion date | December 2016 |
Est. primary completion date | December 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 6 Months to 5 Years |
Eligibility |
Inclusion Criteria: - children (both boys and girls) with SAM defined by WH < -3 Z score of WHO standard, - completed acute (stabilization) phase management, - clinically well, - no edema and regaining appetite and aged 6 to 60 months will be included. - additional enrollment criteria will be as follows: - no signs of concurrent infection, - mothers/caregivers agreed to stay in their current address for next 4 months (for tracking the children) Exclusion Criteria: - failure to obtain consent from parents or caretakers; - children without any fixed address; - children with tuberculosis or any congenital/acquired disorder affecting growth i.e. trisomy-21 or cerebral palsy; - children on an exclusion diet for the treatment of persistent diarrhea, - having history of soy, peanut or milk protein allergy. |
Country | Name | City | State |
---|---|---|---|
Bangladesh | Icddr,B | Dhaka |
Lead Sponsor | Collaborator |
---|---|
International Centre for Diarrhoeal Disease Research, Bangladesh |
Bangladesh,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To compare the efficacy (rate of weight gain) | By 31st December 2014 we shall be able to complete the enrollment, data analyses and preliminary/draft report writting. | 31 December 2014 (up to 3 years) |
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