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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01634009
Other study ID # PR-09038
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received June 12, 2012
Last updated September 21, 2017
Start date July 2012
Est. completion date December 2016

Study information

Verified date June 2016
Source International Centre for Diarrhoeal Disease Research, Bangladesh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Soy-based RUTF (in double blind design)
Soy-based RUTF will be given in double blind manner

Locations

Country Name City State
Bangladesh Icddr,B Dhaka

Sponsors (1)

Lead Sponsor Collaborator
International Centre for Diarrhoeal Disease Research, Bangladesh

Country where clinical trial is conducted

Bangladesh, 

Outcome

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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